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FDA 510(k), K905164, TUBE DECLOGGER
FDA 510(k), K905164, TUBE DECLOGGER
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510(K) Number: K905164
Device Name: TUBE DECLOGGER
Manufacturer: ANDREW J MILLIGAN
Device Classification Name: Tubes, Gastrointestinal (And Accessories)
Regulation Number: KNT
Classification Product Code: KXA
Date Received: 11/16/1990
Decision Date: 02/13/1991
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: TUBE DECLOGGER
Manufacturer: ANDREW J MILLIGAN
Device Classification Name: Tubes, Gastrointestinal (And Accessories)
Regulation Number: KNT
Classification Product Code: KXA
Date Received: 11/16/1990
Decision Date: 02/13/1991
Decision: Substantially Equivalent (SESE)
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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