Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K902386Substantially Equivalent

Model Tm101 Temperature Monitor

Fisher & Paykel Electronics, Ltd., Auckland, New Zealand, NZ / Traditional, Substantially Equivalent

K902386 is the FDA 510(k) clearance record for MODEL TM101 TEMPERATURE MONITOR, a class II device, cleared for Fisher & Paykel Electronics , Ltd. on under FDA product code FLL (Continuous Measurement Thermometer). FDA's definition for product code FLL reads: "A continuous measurement thermometer is a clinical electronic thermometer indicated to measure the body or skin temperature of a person continuously or in specified intervals. Under this regulation, this product code represents non-exempt...". FDA records list 17 510(k) clearances for Fisher & Paykel Electronics , Ltd., from to . As of , FDA records show no recalls naming K902386.

Clearance record

Decision date
Received
(608 days to decision)
Product code
FLL Continuous Measurement Thermometer
Regulation
21 CFR 880.2910
Device class
Class II
Review panel
General Hospital
Applicant
Fisher & Paykel Electronics , Ltd. 25 Carbine Rd. Panmure, Auckland, New Zealand, NZ
Third party review
No

Clearances, product code FLL

Trailing 12 months
2 clearances under product code FLL in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FLL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260