← Back to catalogue
Philips Nm3 Respiratory Monitor With Ventassist
FDA 510(k)Class II (US FDA 510(k))
510(k) K103578
Identifiers
- 510(k) Number
- K103578 FDA 510(k)
- FDA Product Code
- BZK FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 868.1850 FDA 510(k)
- Regulation Number
- 868.1850 FDA 510(k)
- Advisory Committee
- Anesthesiology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Philips Nm3 Respiratory Monitor With Ventassist by Respironics Novametrix, LLC — 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 | K103578 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Respironics Novametrix, LLC
Sources (1)
- FDA 510(k) K103578 24 fields · synced Oct 9, 2026