← Back to catalogue
HOSPIRA LATEX-FREE ADVANCED SENSOR CATHETERS - Hospira Latex-Free Advanced Sensor Catheters
FDA 510(k)Class II (US FDA 510(k))
510(k) K061450
Identifiers
- 510(k) Number
- K061450 FDA 510(k)
- FDA Product Code
- DQE FDA 510(k)
- Models / Variants
- Hospira Latex-Free Advanced Sensor Catheters FDA 510(k)Hospira Latex-Free Critical Care Catheters FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 870.1230 FDA 510(k)
- Regulation Number
- 870.1230 FDA 510(k)
- Advisory Committee
- Cardiovascular FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
HOSPIRA LATEX-FREE ADVANCED SENSOR CATHETERS - Hospira Latex-Free Advanced Sensor Catheters by Hospira, Inc. — Class II — FDA_510K — listed in FDA 510(k) — 2…
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K061450 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Hospira, Inc.
Sources (1)
- FDA 510(k) K061450 24 fields · synced Jun 18, 2026