510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K790121Substantially Equivalent

Film-X 90

Automatic Film Processor Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K790121 is the FDA 510(k) clearance record for FILM-X 90, a class II device, cleared for Automatic Film Processor Corp. on under FDA product code IXW (Processor, Radiographic-Film, Automatic). FDA records list one 510(k) clearance for Automatic Film Processor Corp. As of , FDA records show no recalls naming K790121.

Clearance record

Decision date
Received
(29 days to decision)
Product code
IXW Processor, Radiographic-Film, Automatic
Regulation
21 CFR 892.1900
Device class
Class II
Review panel
Radiology
Applicant
Automatic Film Processor Corp. 803 N. Front St. Suite 3, Mchenry IL
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