510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K221081Substantially Equivalent

iQFlex M Mobile X-ray System, iQFlex MD Mobile X-ray System

First Source Inc, Rochester NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K221081 is the FDA 510(k) clearance record for iQFlex M Mobile X-ray System, iQFlex MD Mobile X-ray System, a class II device, cleared for First Source, Inc. on under FDA product code IZL (System, X-Ray, Mobile). FDA records list 3 510(k) clearances for First Source, Inc., from to . As of , FDA records show one recall naming K221081.

Clearance record

Decision date
Received
(62 days to decision)
Product code
IZL System, X-Ray, Mobile
Regulation
21 CFR 892.1720
Device class
Class II
Review panel
Radiology
Applicant
First Source, Inc. 3495 Winton Pl., Bldg. E, Suite 1, Rochester NY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code IZL

Trailing 12 months
6 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 20260