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FDA 510(k), K913129, ANGIOLAZ ANGIOSCOPE CATHETER
FDA 510(k), K913129, ANGIOLAZ ANGIOSCOPE CATHETER
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510(K) Number: K913129
Device Name: ANGIOLAZ ANGIOSCOPE CATHETER
Manufacturer: ANGIOLAZ, INC.
Device Classification Name: Angioscope
Regulation Number: 876.1500
Classification Product Code: LYK
Date Received: 07/16/1991
Decision Date: 12/27/1991
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: ANGIOLAZ ANGIOSCOPE CATHETER
Manufacturer: ANGIOLAZ, INC.
Device Classification Name: Angioscope
Regulation Number: 876.1500
Classification Product Code: LYK
Date Received: 07/16/1991
Decision Date: 12/27/1991
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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