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FDA 510(k), K012997, COLLATEK FOAM
FDA 510(k), K012997, COLLATEK FOAM
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510(K) Number: K012997
Device Name: COLLATEK FOAM
Manufacturer: BIOCORE MEDICAL TECHNOLOGIES, INC.
Device Classification Name: dressing, wound and burn, occlusive
Regulation Number:
Classification Product Code: MGP
Date Received: 09/06/2001
Decision Date: 10/25/2001
Regulation Medical Specialty:
Device Name: COLLATEK FOAM
Manufacturer: BIOCORE MEDICAL TECHNOLOGIES, INC.
Device Classification Name: dressing, wound and burn, occlusive
Regulation Number:
Classification Product Code: MGP
Date Received: 09/06/2001
Decision Date: 10/25/2001
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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