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FDA 510(k), K965120, ALLCLENZ WOUND CLEANSER
FDA 510(k), K965120, ALLCLENZ WOUND CLEANSER
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$149.00 USD
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510(K) Number: K965120
Device Name: ALLCLENZ WOUND CLEANSER
Manufacturer: DPT LABORATORIES, LTD.
Device Classification Name: bandage, liquid
Regulation Number: 880.5090
Classification Product Code: KMF
Date Received: 12/23/1996
Decision Date: 03/21/1997
Regulation Medical Specialty: General Hospital
Device Name: ALLCLENZ WOUND CLEANSER
Manufacturer: DPT LABORATORIES, LTD.
Device Classification Name: bandage, liquid
Regulation Number: 880.5090
Classification Product Code: KMF
Date Received: 12/23/1996
Decision Date: 03/21/1997
Regulation Medical Specialty: General Hospital
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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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