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FDA 510(k), K003901, ANGIODYNAMICS SOFT-VU SIZING ANGIOGRAPHIC CATHETER
FDA 510(k), K003901, ANGIODYNAMICS SOFT-VU SIZING ANGIOGRAPHIC CATHETER
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510(K) Number: K003901
Device Name: ANGIODYNAMICS SOFT-VU SIZING ANGIOGRAPHIC CATHETER
Manufacturer: ANGIODYNAMICS, INC.
Device Classification Name: catheter, intravascular, diagnostic
Regulation Number: 870.1200
Classification Product Code: DQO
Date Received: 12/18/2000
Decision Date: 01/17/2001
Regulation Medical Specialty: Cardiovascular
Device Name: ANGIODYNAMICS SOFT-VU SIZING ANGIOGRAPHIC CATHETER
Manufacturer: ANGIODYNAMICS, INC.
Device Classification Name: catheter, intravascular, diagnostic
Regulation Number: 870.1200
Classification Product Code: DQO
Date Received: 12/18/2000
Decision Date: 01/17/2001
Regulation Medical Specialty: Cardiovascular
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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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