VJW2919 PNEUMATIC COMPRESSION UPGRADE— 510(k) K920938

Name: FDA 510(k) clearance K920938
Creator: U.S. Food and Drug Administration
Published: 1992-06-17

Substantially Equivalent

Varian Canada, Inc.

FDA 510(k) clearance K920938 for VJW2919 PNEUMATIC COMPRESSION UPGRADE, Substantially Equivalent on 1992-06-17. Applicant: Varian Canada, Inc.. Device class: 2.

Clearance details

Applicant: Varian Canada, Inc.
Product code: Code IZH
Device class: Class 2
Regulation: 21 CFR 892.1710
Advisory panel: Radiology
Date received: 1992-02-27
Decision date: 1992-06-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canada L7g 2j4, CA

Download summary PDF View on FDA.gov ↗

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