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FDA 510(k), K811446, HYDRON WOUND DRESSING KIT
FDA 510(k), K811446, HYDRON WOUND DRESSING KIT
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510(K) Number: K811446
Device Name: HYDRON WOUND DRESSING KIT
Manufacturer:
Device Classification Name: Bandage, Liquid
Regulation Number: KMF
Classification Product Code: KXA
Date Received: 05/22/1981
Decision Date: 06/12/1981
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: HYDRON WOUND DRESSING KIT
Manufacturer:
Device Classification Name: Bandage, Liquid
Regulation Number: KMF
Classification Product Code: KXA
Date Received: 05/22/1981
Decision Date: 06/12/1981
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
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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. Learn more about Fast-Track Requests here.
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