Identifiers
- 510(k) Number
- K180757 FDA 510(k)
- FDA Product Code
- HCH FDA 510(k)
- Models / Variants
- D-Clip FDA 510(k)D-Clip Applier FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 882.5200 FDA 510(k)
- Regulation Number
- 882.5200 FDA 510(k)
- Advisory Committee
- Neurology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
D-Clip +1 more model by Peter Lazic GmbH — Class II — FDA_510K — listed in FDA 510(k) — 2 models — 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 | K180757 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Peter Lazic GmbH
Sources (1)
- FDA 510(k) K180757 24 fields · synced Jun 19, 2026