510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K912225Substantially Equivalent

3M Digital Recording Automatic Film Handling Unit

3M Medical Products Group, St Paul MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K912225 is the FDA 510(k) clearance record for 3M DIGITAL RECORDING AUTOMATIC FILM HANDLING UNIT, a class II device, cleared for 3M Medical Products Group on under FDA product code IXW (Processor, Radiographic-Film, Automatic). FDA records list 12 510(k) clearances for 3M Medical Products Group, from to . As of , FDA records show no recalls naming K912225.

Clearance record

Decision date
Received
(63 days to decision)
Product code
IXW Processor, Radiographic-Film, Automatic
Regulation
21 CFR 892.1900
Device class
Class II
Review panel
Radiology
Applicant
3M Medical Products Group 3m Center, Bldg. 275-3e-08, St Paul MN
510(k) summary
Summary
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