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
K790673Substantially Equivalent

Omnimedical Automatic 1001

Omnimedical, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K790673 is the FDA 510(k) clearance record for OMNIMEDICAL AUTOMATIC 1001, a class II device, cleared for Omnimedical on under FDA product code IZL (System, X-Ray, Mobile). FDA records list 6 510(k) clearances for Omnimedical, from to . As of , FDA records show no recalls naming K790673.

Clearance record

Decision date
Received
(25 days to decision)
Product code
IZL System, X-Ray, Mobile
Regulation
21 CFR 892.1720
Device class
Class II
Review panel
Radiology
Applicant
Omnimedical 803 N. Front St. Suite 3, Mchenry IL
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