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FDA 510(k), K925914, PRE-TIED LOOP SUTURE CANNULA
FDA 510(k), K925914, PRE-TIED LOOP SUTURE CANNULA
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510(K) Number: K925914
Device Name: PRE-TIED LOOP SUTURE CANNULA
Manufacturer: JOHN D PAULSON
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: GCJ
Classification Product Code: 11/23/1992
Date Received: 05/12/1993
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: PRE-TIED LOOP SUTURE CANNULA
Manufacturer: JOHN D PAULSON
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: GCJ
Classification Product Code: 11/23/1992
Date Received: 05/12/1993
Decision Date: Substantially Equivalent (SESE)
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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