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FDA 510(k), K032948, ELASTIC SKIN LIQUID BANDAGE
FDA 510(k), K032948, ELASTIC SKIN LIQUID BANDAGE
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510(K) Number: K032948
Device Name: ELASTIC SKIN LIQUID BANDAGE
Manufacturer: JOSEPH G SANT'ANGELO
Device Classification Name: Bandage, Liquid
Regulation Number: KMF
Classification Product Code: 09/22/2003
Date Received: 06/25/2004
Decision Date: SE - With Limitations (SESU)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: ELASTIC SKIN LIQUID BANDAGE
Manufacturer: JOSEPH G SANT'ANGELO
Device Classification Name: Bandage, Liquid
Regulation Number: KMF
Classification Product Code: 09/22/2003
Date Received: 06/25/2004
Decision Date: SE - With Limitations (SESU)
Regulation Medical Specialty: General & Plastic Surgery
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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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