QuikClot Control+ Hemostatic Device— 510(k) K243553
Substantially EquivalentTeleflex Medical
FDA 510(k) clearance K243553 for QuikClot Control+ Hemostatic Device, Substantially Equivalent on 2025-03-18. Applicant: Teleflex Medical. Device class: 2.
Clearance details
- Applicant
- Teleflex Medical
- Product code
- Code POD
- Device class
- Class 2
- Regulation
- 21 CFR 878.4454
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Morrisville, NC, US
Recent devices under product code POD
view allMore clearances from Teleflex Medical
view allData sourced from openFDA. This site is unofficial and independent of the FDA.