• FDA DYMISTA NDA 202236 approval records — 22 FDA documents, 848 pages
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FDA 510(k) K964034, TRANSJUGULAR ACCESS SET, by AngioDynamics, Inc.

FDA 510(k) K964034, TRANSJUGULAR ACCESS SET, by AngioDynamics, Inc.

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510(K) Number: K964034
Device Name: TRANSJUGULAR ACCESS SET
Manufacturer: AngioDynamics, Inc.
Device Classification Name: introducer, catheter
Regulation Number: 870.1340
Classification Product Code: DYB
Date Received: 10/08/1996
Decision Date: 05/06/1997
Regulation Medical Specialty: Cardiovascular
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