AVD INTIMAX OCCLUSION CATHETER— 510(k) K910339

Substantially Equivalent

Applied Vascular Devices, Inc.

FDA 510(k) clearance K910339 for AVD INTIMAX OCCLUSION CATHETER, Substantially Equivalent on 1991-05-29. Applicant: Applied Vascular Devices, Inc..

Clearance details

Applicant: Applied Vascular Devices, Inc.
Product code: Code DQT
Advisory panel: Cardiovascular
Date received: 1991-01-28
Decision date: 1991-05-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Laguna Hills, CA, US

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