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FDA 510(k), K946357, COLLAGEN INTRACANALICULAR PLUG
FDA 510(k), K946357, COLLAGEN INTRACANALICULAR PLUG
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510(K) Number: K946357
Device Name: COLLAGEN INTRACANALICULAR PLUG
Manufacturer: OASIS MEDICAL, INC.
Device Classification Name: plug, punctum
Regulation Number:
Classification Product Code: LZU
Date Received: 12/30/1994
Decision Date: 02/07/1995
Regulation Medical Specialty:
Device Name: COLLAGEN INTRACANALICULAR PLUG
Manufacturer: OASIS MEDICAL, INC.
Device Classification Name: plug, punctum
Regulation Number:
Classification Product Code: LZU
Date Received: 12/30/1994
Decision Date: 02/07/1995
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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