510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K953250Substantially Equivalent

Senographe Pearl and Senographe Sapphire

GE Healthcare, Milwaukee WI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K953250 is the FDA 510(k) clearance record for SENOGRAPHE PEARL AND SENOGRAPHE SAPPHIRE, a class II device, cleared for GE Medical Systems on under FDA product code IZH (System, X-Ray, Mammographic). FDA records list 888 510(k) clearances for GE HEALTHCARE, from to . As of , FDA records show 2 recalls naming K953250.

Clearance record

Decision date
Received
(198 days to decision)
Product code
IZH System, X-Ray, Mammographic
Regulation
21 CFR 892.1710
Device class
Class II
Review panel
Radiology
Applicant
GE Medical Systems P.o. 414, Milwaukee WI
510(k) summary
Summary
Third party review
No

Clearances, product code IZH

Trailing 12 months

FDA records hold no clearances under product code IZH in the trailing twelve months.

FDA records show no clearances under product code IZH in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code IZH, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260