AD/V A.5— 510(k) K925799

Substantially Equivalent

Adaptive Video, Inc.

FDA 510(k) clearance K925799 for AD/V A.5, Substantially Equivalent on 1994-02-18. Applicant: Adaptive Video, Inc.. Device class: 2.

Clearance details

Applicant: Adaptive Video, Inc.
Product code: Code LMA
Device class: Class 2
Regulation: 21 CFR 892.2030
Advisory panel: Radiology
Date received: 1992-11-16
Decision date: 1994-02-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Novato, CA, US

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More clearances from Adaptive Video, Inc.

K943158 — AD/V IMAGEPLEX(TM)1994-11-22
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Data sourced from openFDA. This site is unofficial and independent of the FDA.