← Back to catalogue
Mk-Dent Low Speed Handpieces And Accessories Including Spare Parts, Tubings, An…
FDA 510(k)Class I (US FDA 510(k))
510(k) K051872
by MK-Dent GmbH
Identifiers
- 510(k) Number
- K051872 FDA 510(k)
- FDA Product Code
- EFB FDA 510(k)
Classification
- Device Class
- Class I FDA 510(k)
- Legislation / Framework
- 21 CFR Part 872.4200 FDA 510(k)
- Regulation Number
- 872.4200 FDA 510(k)
- Advisory Committee
- Dental FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Mk-Dent Low Speed Handpieces And Accessories Including Spare Parts, Tubings, An… by MK-Dent GmbH — Class I — FDA_510K — listed in FDA 510(k)
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 | K051872 | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- MK-Dent GmbH
Sources (1)
- FDA 510(k) K051872 24 fields · synced Jun 18, 2026