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FDA 510(k), K900123, AUTO SUTURE SURGIPORT SPIRAL SLEEVE
FDA 510(k), K900123, AUTO SUTURE SURGIPORT SPIRAL SLEEVE
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510(K) Number: K900123
Device Name: AUTO SUTURE SURGIPORT SPIRAL SLEEVE
Manufacturer: CURTIS RAYMOND
Device Classification Name: Trocar, Gastro-Urology
Regulation Number: FBQ
Classification Product Code: 01/09/1990
Date Received: 04/04/1990
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: AUTO SUTURE SURGIPORT SPIRAL SLEEVE
Manufacturer: CURTIS RAYMOND
Device Classification Name: Trocar, Gastro-Urology
Regulation Number: FBQ
Classification Product Code: 01/09/1990
Date Received: 04/04/1990
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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