← Back to catalogue
General Patient Monitors, Models: G3c/ G3d/ G3f/ G3g/ G3h
FDA 510(k)Class II (US FDA 510(k))
510(k) K092970
Identifiers
- 510(k) Number
- K092970 FDA 510(k)
- FDA Product Code
- MHX FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 870.1025 FDA 510(k)
- Regulation Number
- 870.1025 FDA 510(k)
- Advisory Committee
- Cardiovascular FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
General Patient Monitors, Models: G3c/ G3d/ G3f/ G3g/ G3h by General Meditech, Inc. — Class II — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS
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 | K092970 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- General Meditech, Inc.
Sources (1)
- FDA 510(k) K092970 24 fields · synced Jun 18, 2026