FDA 510(k), K220971, QuikClot Control+ Hemostatic Dressing
FDA 510(k), K220971, QuikClot Control+ Hemostatic Dressing
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510(K) Number: K220971
Device Name: QuikClot Control+ Hemostatic Dressing
Manufacturer: Soraya King
Device Classification Name: Temporary, Internal Use Hemostatic
Regulation Number: POD
Classification Product Code: 04/04/2022
Date Received: 12/14/2022
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: QuikClot Control+ Hemostatic Dressing
Manufacturer: Soraya King
Device Classification Name: Temporary, Internal Use Hemostatic
Regulation Number: POD
Classification Product Code: 04/04/2022
Date Received: 12/14/2022
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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