Pollenex Digital Thermometer T-225

FDA 510(k) K850363 · Associated Mills, Inc.

Substantially Equivalent

510(k) numberK850363

Submission

Device name
Pollenex Digital Thermometer T-225
Applicant
Associated Mills, Inc.
Chicago, IL, US
Received
January 30, 1985
Decision date
February 15, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FLL – Continuous Measurement Thermometer
Device class
Class II (moderate risk)
Regulation
21 CFR 880.2910
Specialty
General Hospital

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 devices. For more information, see 90 FR 25889, available at https://www.govinfo.gov/content/pkg/FR-2025-06-18/pdf/2025-11207.pdf.

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Questions and answers

When was Pollenex Digital Thermometer T-225 cleared by the FDA?

Pollenex Digital Thermometer T-225 (K850363) received a 510(k) decision of Substantially Equivalent on February 15, 1985, 16 days after the submission was received.

What is the product code of K850363?

The FDA product code is FLL – Continuous Measurement Thermometer, a Class II (moderate risk) device regulated under 21 CFR 880.2910.