510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K061361Substantially Equivalent

Faxitron Digital Radiography System, Model Dx-50

Faxitron X-Ray Corp., Wheeling IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K061361 is the FDA 510(k) clearance record for FAXITRON DIGITAL RADIOGRAPHY SYSTEM, MODEL DX-50, a class II device, cleared for Faxitron X-Ray Corp. on under FDA product code MWP (Cabinet, X-Ray System). FDA records list 2 510(k) clearances for Faxitron X-Ray Corp., from to . As of , FDA records show no recalls naming K061361.

Clearance record

Decision date
Received
(91 days to decision)
Product code
MWP Cabinet, X-Ray System
Regulation
21 CFR 892.1680
Device class
Class II
Review panel
Radiology
Applicant
Faxitron X-Ray Corp. 225 Larkin Dr.,Suite 1, Wheeling IL
510(k) summary
Statement
Third party review
No

Clearances, product code MWP

Trailing 12 months

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

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