Radius T wearable thermometer

FDA 510(k) K203215 · Masimo Corporation

Substantially Equivalent

510(k) numberK203215

Submission

Device name
Radius T wearable thermometer
Applicant
Masimo Corporation
Irvine, CA, US
Received
November 2, 2020
Decision date
June 11, 2021
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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 Radius T wearable thermometer cleared by the FDA?

Radius T wearable thermometer (K203215) received a 510(k) decision of Substantially Equivalent on June 11, 2021, 221 days after the submission was received.

What is the product code of K203215?

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