K232970
- 510(k) number
- K232970
- Device name
- Hem-o-lok® Ligating Clips
- Applicant
- Teleflex Medical NC · US
- Product code
- FZP — Clip, Implantable
- Decision date
- 2024-01-12
- Date received
- 2023-09-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K232970.pdf
Official FDA record: K232970
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.