510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K940112Substantially Equivalent

X-Ray Film Processor

Fischer Industries, Inc., Geneva IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K940112 is the FDA 510(k) clearance record for X-RAY FILM PROCESSOR, a class II device, cleared for Fischer Industries, Inc. on under FDA product code IXW (Processor, Radiographic-Film, Automatic). FDA records list 3 510(k) clearances for Fischer Industries, Inc., from to . As of , FDA records show no recalls naming K940112.

Clearance record

Decision date
Received
(456 days to decision)
Product code
IXW Processor, Radiographic-Film, Automatic
Regulation
21 CFR 892.1900
Device class
Class II
Review panel
Radiology
Applicant
Fischer Industries, Inc. 2630 Kaneville Ct., Geneva IL
510(k) summary
Statement
Third party review
No

Clearances, product code IXW

Trailing 12 months

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

FDA records show no clearances under product code IXW in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code IXW, 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