Rectal Temp. Telemetry Monitor

FDA 510(k) K832404 · Xomed, Inc.

Substantially Equivalent

510(k) numberK832404

Submission

Device name
Rectal Temp. Telemetry Monitor
Applicant
Xomed, Inc.
Arnold, MO, US
Received
July 20, 1983
Decision date
September 12, 1983
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 Rectal Temp. Telemetry Monitor cleared by the FDA?

Rectal Temp. Telemetry Monitor (K832404) received a 510(k) decision of Substantially Equivalent on September 12, 1983, 54 days after the submission was received.

What is the product code of K832404?

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