DeRoyal Temperature Monitoring Probe

FDA 510(k) K200631 · Deroyal Industries, Inc.

Substantially Equivalent

510(k) numberK200631

Submission

Device name
DeRoyal Temperature Monitoring Probe
Applicant
Deroyal Industries, Inc.
Powell, TN, US
Received
March 10, 2020
Decision date
December 23, 2020
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 DeRoyal Temperature Monitoring Probe cleared by the FDA?

DeRoyal Temperature Monitoring Probe (K200631) received a 510(k) decision of Substantially Equivalent on December 23, 2020, 288 days after the submission was received.

What is the product code of K200631?

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