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FDA 510(k), K840568, ACTIVE LIFE ONE-PIECE CLOSED-END POUCH
FDA 510(k), K840568, ACTIVE LIFE ONE-PIECE CLOSED-END POUCH
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510(K) Number: K840568
Device Name: ACTIVE LIFE ONE-PIECE CLOSED-END POUCH
Manufacturer: CONVATEC, A DIVISION OF E.R. SQUIBB & SONS
Device Classification Name: collector, ostomy
Regulation Number: 876.5900
Classification Product Code: EXB
Date Received: 02/08/1984
Decision Date: 05/02/1984
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: ACTIVE LIFE ONE-PIECE CLOSED-END POUCH
Manufacturer: CONVATEC, A DIVISION OF E.R. SQUIBB & SONS
Device Classification Name: collector, ostomy
Regulation Number: 876.5900
Classification Product Code: EXB
Date Received: 02/08/1984
Decision Date: 05/02/1984
Regulation Medical Specialty: Gastroenterology/Urology
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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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