Electromedics HG (Hydrogel) Series Skin Temperature Sensor

FDA 510(k) K933832 · Electromedics, Inc.

Substantially Equivalent

510(k) numberK933832

Submission

Device name
Electromedics HG (Hydrogel) Series Skin Temperature Sensor
Applicant
Electromedics, Inc.
Englewood, CO, US
Received
August 5, 1993
Decision date
January 28, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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 Electromedics HG (Hydrogel) Series Skin Temperature Sensor cleared by the FDA?

Electromedics HG (Hydrogel) Series Skin Temperature Sensor (K933832) received a 510(k) decision of Substantially Equivalent on January 28, 1994, 176 days after the submission was received.

What is the product code of K933832?

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