510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K920938Substantially Equivalent

Vjw2919 Pneumatic Compression Upgrade

Varian Canada, Inc., Canada L7g 2j4, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K920938 is the FDA 510(k) clearance record for VJW2919 PNEUMATIC COMPRESSION UPGRADE, a class II device, cleared for Varian Canada, Inc. on under FDA product code IZH (System, X-Ray, Mammographic). FDA records list 7 510(k) clearances for Varian Canada, Inc., from to . As of , FDA records show no recalls naming K920938.

Clearance record

Decision date
Received
(111 days to decision)
Product code
IZH System, X-Ray, Mammographic
Regulation
21 CFR 892.1710
Device class
Class II
Review panel
Radiology
Applicant
Varian Canada, Inc. 45 River Dr., Canada L7g 2j4, CA
510(k) summary
Statement
Third party review
No

Clearances, product code IZH

Trailing 12 months

FDA records hold no clearances under product code IZH in the trailing twelve months.

FDA records show no clearances under product code IZH in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code IZH, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260