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FDA 510(k), K110386, CELOX RAPID GAUZE
FDA 510(k), K110386, CELOX RAPID GAUZE
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510(K) Number: K110386
Device Name: CELOX RAPID GAUZE
Manufacturer: MEDTRADE PRODUCTS LTD.
Device Classification Name: hemostatic wound dressing without thrombin or other biologics
Regulation Number:
Classification Product Code: QSY
Date Received: 02/10/2011
Decision Date: 05/10/2011
Regulation Medical Specialty:
Device Name: CELOX RAPID GAUZE
Manufacturer: MEDTRADE PRODUCTS LTD.
Device Classification Name: hemostatic wound dressing without thrombin or other biologics
Regulation Number:
Classification Product Code: QSY
Date Received: 02/10/2011
Decision Date: 05/10/2011
Regulation Medical Specialty:
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- 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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