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Sign in to claim this brandMichigan Critical Care Consultants, Inc. (D.B.A Mc3 Inc.)
US
Last updated May 23, 2026
What Michigan Critical Care Consultants, Inc. (D.B.A Mc3 Inc.) makes
Michigan Critical Care Consultants, Inc. manufactures medical devices for critical care environments, including the VitalFlow Console—a system for managing patient ventilation—and the VitalFlow Centrifugal Pump, designed for precise fluid administration in intensive care settings.
The company’s portfolio is regulated under FDA’s Class II device classification, with products authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) database, and the manufacturer operates from the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Michigan Critical Care Consultants, Inc. (D.B.A Mc3 Inc.) manufacture?
Michigan Critical Care Consultants, Inc. designs medical devices specifically for critical care settings. Their portfolio includes systems like the VitalFlow Console, which supports patient ventilation management, and the VitalFlow Centrifugal Pump, used for precise fluid administration in intensive care. These devices are engineered to address critical care needs with advanced functionality.
Where is Michigan Critical Care Consultants, Inc. based?
The company is headquartered in the United States. While the exact location isn’t specified, its operations and regulatory filings are conducted within the country, aligning with U.S. medical device compliance standards.
How are Michigan Critical Care Consultants, Inc.’s devices classified by regulatory authorities?
The company’s devices fall under the FDA’s Class II classification, indicating moderate risk and requiring premarket notification (510(k)) clearance before commercial distribution. This classification reflects the need for validation of safety and performance in critical care applications.
Are Michigan Critical Care Consultants, Inc.’s devices listed in any regulatory databases?
Yes, the company’s devices are included in the FDA’s 510(k) database, where authorised products are recorded. This listing confirms that each device has undergone the required regulatory review process (510(k) pathway) to demonstrate substantial equivalence to a legally marketed predicate device.
AI-generated from registry data and not verified by a human reviewer.
Information
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Catalogue (79)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Mc3 | 6386 | FDA UDI | Class II | Active |
| Mc3 | 7071 | FDA UDI | Class II | Active |
| MC3 Crescent RA Dual Lumen Catheter 19FR | 70419 | FDA UDI | Class II | Active |
| Michigan Critical Care Consultants, Inc. | 7072 | FDA UDI | Class II | Active |
| Mc3 | 4949 | FDA UDI | Class II | Active |
| Mc3 | 5768 | FDA UDI | Class II | Active |
| Michigan Critical Care Consultants, Inc. | 6392 | FDA UDI | Class II | Active |
| MC3 Crescent Jugular Dual Lumen Catheter | 70130 | FDA UDI | Class II | Active |
| MC3 Crescent RA Dual Lumen Catheter 15FR | 70415 | FDA UDI | Class II | Active |
| VitalFlow Centrifugal Pump | 58111 | FDA UDI | Class II | Active |
| VitalFlow Motor Drive | 58102 | FDA UDI | Class II | Active |
| VitalFlow Caddy | 58120 | FDA UDI | Class I | Active |
| MC3 Nautilus (tm) Smart ECMO Module | 48135 | FDA UDI | Class II | Active |
| MC3 Crescent RA Dual Lumen Catheter 13FR | 70413 | FDA UDI | Class II | Active |
| MC3 Nautilus ECMO Oxygenator | 48145E | FDA UDI | Class II | Active |
| MC3 Crescent(tm) Jugular Dual Lumen Catheter 24 FR | 70124 | FDA UDI | Class II | Active |
| Michigan Critical Care Consultants, Inc. | 5843 | FDA UDI | Class II | Active |
| VitalFlow Power Cord 12 V DC, 3m | 58141 | FDA UDI | Class II | Active |
| VitalFlow Power Cord CEE 7/7, 2.5m | 58132 | FDA UDI | Class II | Active |
| Mc3 | 5843 | FDA UDI | Class II | Active |
| MC3 Nautilus(tm) Smart Power Supply 12VDC | 48150 | FDA UDI | Class II | Active |
| Michigan Critical Care Consultants, Inc. | 5762 | FDA UDI | Class II | Active |
| MC3 Crescent(tm) Jugular Dual Lumen Catheter | 70130 | FDA UDI | Class II | Active |
| Mc3 | 5767 | FDA UDI | Class II | Active |
| MC3 Opus(tm) Vascular Access Kit | 21030 | FDA UDI | Class II | Active |
| VitalFlow Flow and Bubble Sensor, 2m | 58150 | FDA UDI | Class II | Active |
| MC3 Crescent Jugular Dual Lumen Catheter | 70126 | FDA UDI | Class II | Active |
| VitalFlow™ Console | K230364 | FDA 510(k) | Class II | Active |
| VitalFlowTM Centrifugal Pump | K223898 | FDA 510(k) | Class II | Active |
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