510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K082185Substantially Equivalent

Ge Logiq E9 Diagnostic Ultrasound System, Models 5205000, 5205000-2

GE Medical Systems Ultrasound and Primary Care Dia, Wauwatosa WI / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K082185 is the FDA 510(k) clearance record for GE LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM, MODELS 5205000, 5205000-2, a class II device, cleared for Ge Medical Systems Ultrasound and Primary Care Dia on under FDA product code IYO (System, Imaging, Pulsed Echo, Ultrasonic). FDA records list 7 510(k) clearances for Ge Medical Systems Ultrasound and Primary Care Dia, from to . As of , FDA records show one recall naming K082185.

Clearance record

Decision date
Received
(14 days to decision)
Product code
IYO System, Imaging, Pulsed Echo, Ultrasonic
Regulation
21 CFR 892.1560
Device class
Class II
Review panel
Radiology
Applicant
Ge Medical Systems Ultrasound and Primary Care Dia 9900 Innovation Dr., Wauwatosa WI
510(k) summary
Summary PDF
Third party review
No

Clearances, product code IYO

Trailing 12 months
8 clearances under product code IYO in the twelve months to October 2026, February 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code IYO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20262
March 20261
April 20262
May 20260
June 20261
July 20261
August 20260
September 20261
October 20260