← Back to catalogue
Instruments For One Time Use/ Disposable
FDA 510(k)Class I (US FDA 510(k))
510(k) K903962
Identifiers
- 510(k) Number
- K903962 FDA 510(k)
- FDA Product Code
- LRP FDA 510(k)
Classification
- Device Class
- Class I FDA 510(k)
- Legislation / Framework
- 21 CFR Part 878.4800 FDA 510(k)
- Regulation Number
- 878.4800 FDA 510(k)
- Advisory Committee
- General, Plastic Surgery FDA 510(k)
- FDA Decision
- SEKD FDA 510(k)
Instruments For One Time Use/ Disposable by Apk Technology — Class I — 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 | K903962 | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Apk Technology
Sources (1)
- FDA 510(k) K903962 24 fields · synced Jun 19, 2026