K243553
- 510(k) number
- K243553
- Device name
- QuikClot Control+ Hemostatic Device
- Applicant
- Teleflex Medical NC · US
- Product code
- POD — Temporary, Internal Use Hemostatic
- Decision date
- 2025-03-18
- Date received
- 2024-11-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 3.5 MB · U.S. public domain
Also available from FDA: K243553.pdf
Official FDA record: K243553
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.