510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K090697Substantially Equivalent

Modification to: Giraffe and Panda Warmer

GE Healthcare, Laurel MD / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K090697 is the FDA 510(k) clearance record for MODIFICATION TO: GIRAFFE AND PANDA WARMER, a class II device, cleared for Ohmeda Medical on under FDA product code FMT (Warmer, Infant Radiant). FDA records list 888 510(k) clearances for GE HEALTHCARE, from to . As of , FDA records show 6 recalls naming K090697.

Clearance record

Decision date
Received
(30 days to decision)
Product code
FMT Warmer, Infant Radiant
Regulation
21 CFR 880.5130
Device class
Class II
Review panel
General Hospital
Applicant
Ohmeda Medical 8880 Gorman Rd., Laurel MD
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FMT

Trailing 12 months

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

FDA records show no clearances under product code FMT in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FMT, 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