Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K200319Substantially Equivalent

HYDRO-TEMP Neonatal Skin Surface Temperature Sensor, HYDRO-TEMP Neonatal Skin Surface Temperature Sensor with Interface Cable

DeRoyal Industries, Inc., Powell TN / Traditional, Substantially Equivalent

K200319 is the FDA 510(k) clearance record for HYDRO-TEMP Neonatal Skin Surface Temperature Sensor, HYDRO-TEMP Neonatal Skin Surface Temperature Sensor with Interface Cable, a class II device, cleared for Deroyal Industries, Inc. on under FDA product code FMT (Warmer, Infant Radiant). FDA records list 92 510(k) clearances for Deroyal Industries, Inc., from to . As of , FDA records show no recalls naming K200319.

Clearance record

Decision date
Received
(55 days to decision)
Product code
FMT Warmer, Infant Radiant
Regulation
21 CFR 880.5130
Device class
Class II
Review panel
General Hospital
Applicant
Deroyal Industries, Inc. 200 Debusk Ln., Powell TN
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