Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K121625Substantially Equivalent

Lullaby Tm Warmer

Wipro GE Healthcare Private Ltd., Laurel MD / Traditional, Substantially Equivalent

K121625 is the FDA 510(k) clearance record for LULLABY TM WARMER, a class II device, cleared for Wipro GE Healthcare Private, Ltd. on under FDA product code FMT (Warmer, Infant Radiant). FDA records list 5 510(k) clearances for Wipro GE Healthcare Private, Ltd., from to . As of , FDA records show no recalls naming K121625.

Clearance record

Decision date
Received
(105 days to decision)
Product code
FMT Warmer, Infant Radiant
Regulation
21 CFR 880.5130
Device class
Class II
Review panel
General Hospital
Applicant
Wipro GE Healthcare Private, Ltd. 8880 Goman 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