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FDA 510(k), K951104, ENDOBOOT
FDA 510(k), K951104, ENDOBOOT
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$149.00 USD
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510(K) Number: K951104
Device Name: ENDOBOOT
Manufacturer: UNITED STATES ENDOSCOPY GROUP, INC.
Device Classification Name: endoscopic storage cover
Regulation Number: 876.1500
Classification Product Code: OCU
Date Received: 03/10/1995
Decision Date: 04/06/1995
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: ENDOBOOT
Manufacturer: UNITED STATES ENDOSCOPY GROUP, INC.
Device Classification Name: endoscopic storage cover
Regulation Number: 876.1500
Classification Product Code: OCU
Date Received: 03/10/1995
Decision Date: 04/06/1995
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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