510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K941931Substantially Equivalent

Diagnostic X-Ray Patient Exposure Indicator

Victoreen, Inc., Solon OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K941931 is the FDA 510(k) clearance record for DIAGNOSTIC X-RAY PATIENT EXPOSURE INDICATOR, a class II device, cleared for Victoreen, Inc. on under FDA product code KPR (System, X-Ray, Stationary). FDA records list 40 510(k) clearances for Victoreen, Inc., from to . As of , FDA records show no recalls naming K941931.

Clearance record

Decision date
Received
(36 days to decision)
Product code
KPR System, X-Ray, Stationary
Regulation
21 CFR 892.1680
Device class
Class II
Review panel
Radiology
Applicant
Victoreen, Inc. 6000 Cochran Rd., Solon OH
510(k) summary
Statement
Third party review
No

Clearances, product code KPR

Trailing 12 months
7 clearances under product code KPR in the twelve months to October 2026, August 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code KPR, trailing twelve months
MonthClearances
November 20251
December 20250
January 20261
February 20260
March 20260
April 20261
May 20260
June 20261
July 20260
August 20262
September 20261
October 20260