ri-former Predictive Thermometer

FDA 510(k) K171182 · Rudolf Riester GmbH

Substantially Equivalent

510(k) numberK171182

Submission

Device name
ri-former Predictive Thermometer
Applicant
Rudolf Riester GmbH
Junginge, DE
Received
April 24, 2017
Decision date
October 4, 2017
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.

Other 510(k)s with product code FLL

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K250401AION TempShield™FLL · Traditional Aion Biosystems, Inc.03/14/2025SE
K243136Non-contact Forehead Infrared Thermometer (FC-IR2000, FC-IR205, FC-IR202, FC-IR206…FLL · Traditional Shenzhen Finicare Co., Ltd.02/14/2025SE
K240333Wearable Digital Thermometer (T31)FLL · Traditional Guangdong Genial Technology Co., Ltd.10/30/2024SE
K240223FMT Disposable and Autoclavable Temperature ProbesFLL · Traditional Metko Medikal VE Tibbi Cihazlar Dis Ticaret…10/25/2024SE

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Questions and answers

When was ri-former Predictive Thermometer cleared by the FDA?

ri-former Predictive Thermometer (K171182) received a 510(k) decision of Substantially Equivalent on October 4, 2017, 163 days after the submission was received.

What is the product code of K171182?

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