510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K902984Substantially Equivalent

G.e. Amx 110, Amx II and Amx 3 X-Ray Units

Electromek Diagnostic Systems, Inc., Troy IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902984 is the FDA 510(k) clearance record for G.E. AMX 110, AMX II AND AMX 3 X-RAY UNITS, a class II device, cleared for Electromek Diagnostic Systems, Inc. on under FDA product code IZL (System, X-Ray, Mobile). FDA records list 11 510(k) clearances for Electromek Diagnostic Systems, Inc., from to . As of , FDA records show no recalls naming K902984.

Clearance record

Decision date
Received
(122 days to decision)
Product code
IZL System, X-Ray, Mobile
Regulation
21 CFR 892.1720
Device class
Class II
Review panel
Radiology
Applicant
Electromek Diagnostic Systems, Inc. 412 Rte. 40 W., Troy 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