510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K930049Substantially Equivalent

Infrared Exposure Hand Switch

Mid X-Ray, Inc., Hazlet NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930049 is the FDA 510(k) clearance record for INFRARED EXPOSURE HAND SWITCH, a class II device, cleared for Mid X-Ray, Inc. on under FDA product code IZL (System, X-Ray, Mobile). FDA records list one 510(k) clearance for Mid X-Ray, Inc. As of , FDA records show no recalls naming K930049.

Clearance record

Decision date
Received
(168 days to decision)
Product code
IZL System, X-Ray, Mobile
Regulation
21 CFR 892.1720
Device class
Class II
Review panel
Radiology
Applicant
Mid X-Ray, Inc. 115 Clark St., Hazlet NJ
510(k) summary
Summary
Third party review
No

Clearances, product code IZL

Trailing 12 months
7 clearances under product code IZL in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code IZL, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20261
April 20260
May 20261
June 20261
July 20260
August 20261
September 20260
October 20261