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FDA 510(k), K934696, ANGIOSCOPE
FDA 510(k), K934696, ANGIOSCOPE
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510(K) Number: K934696
Device Name: ANGIOSCOPE
Manufacturer: INTRAMED LABORATORIES, INC.
Device Classification Name: Angioscope
Regulation Number: 876.1500
Classification Product Code: LYK
Date Received: 09/30/1993
Decision Date: 01/18/1994
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: ANGIOSCOPE
Manufacturer: INTRAMED LABORATORIES, INC.
Device Classification Name: Angioscope
Regulation Number: 876.1500
Classification Product Code: LYK
Date Received: 09/30/1993
Decision Date: 01/18/1994
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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