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FDA 510(k), K123387, QUIKCLOT HEMOSTATIC DRESSING
FDA 510(k), K123387, QUIKCLOT HEMOSTATIC DRESSING
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510(K) Number: K123387
Device Name: QUIKCLOT HEMOSTATIC DRESSING
Manufacturer: Z-MEDICA, LLC
Device Classification Name: hemostatic wound dressing without thrombin or other biologics
Regulation Number:
Classification Product Code: QSY
Date Received: 11/02/2012
Decision Date: 04/12/2013
Regulation Medical Specialty:
Device Name: QUIKCLOT HEMOSTATIC DRESSING
Manufacturer: Z-MEDICA, LLC
Device Classification Name: hemostatic wound dressing without thrombin or other biologics
Regulation Number:
Classification Product Code: QSY
Date Received: 11/02/2012
Decision Date: 04/12/2013
Regulation Medical Specialty:
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.
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