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LigaSure Retractable L-Hook Laparoscopic Sealer/Divider
FDA 510(k)Class II (US FDA 510(k))
510(k) K161804
by Covidien
Identifiers
- 510(k) Number
- K161804 FDA 510(k)
- FDA Product Code
- GEI FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 878.4400 FDA 510(k)
- Regulation Number
- 878.4400 FDA 510(k)
- Advisory Committee
- General, Plastic Surgery FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
A comprehensive 2-3 paragraph SEO description written in clear, natural language. It explains the key features of this product and its benefits for patients.
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 | K161804 | Class II | Active |
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Manufacturer
- Manufacturer
- Covidien
Sources (1)
- FDA 510(k) K161804 24 fields · synced Jul 12, 2026