AD/V IMAGEPLEX(TM)— 510(k) K943158

Substantially Equivalent

Adaptive Video, Inc.

FDA 510(k) clearance K943158 for AD/V IMAGEPLEX(TM), Substantially Equivalent on 1994-11-22. Applicant: Adaptive Video, Inc.. Device class: 1.

Clearance details

Applicant: Adaptive Video, Inc.
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1994-07-01
Decision date: 1994-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Novato, CA, US

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More clearances from Adaptive Video, Inc.

K925799 — AD/V A.51994-02-18
K921877 — AD/V SPOOLER1992-07-01

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