510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K914005Substantially Equivalent

Fiberoptic Tympanic Thermometer, Model 6000

Daily Medical Products, Inc., San Diego CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K914005 is the FDA 510(k) clearance record for FIBEROPTIC TYMPANIC THERMOMETER, MODEL 6000, a class II device, cleared for Daily Medical Products, Inc. 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 8 510(k) clearances for Daily Medical Products, Inc., from to . As of , FDA records show no recalls naming K914005.

Clearance record

Decision date
Received
(328 days to decision)
Product code
FLL Continuous Measurement Thermometer
Regulation
21 CFR 880.2910
Device class
Class II
Review panel
General Hospital
Applicant
Daily Medical Products, Inc. 3665 Kearny Villa Rd., San Diego CA
510(k) summary
Statement
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