FDA 510(k)

ri-former Predictive Thermometer

Número K: K171182 · 2017-10-04

Data da decisão2017-10-04

Código do produtoFLL

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

ri-former Predictive Thermometer is the device name listed in this FDA 510(k) record. The listed applicant is Rudolf Riester GmbH. It received FDA 510(k) clearance on 2017-10-04 under 510(k) number K171182. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the ri-former Predictive Thermometer?

ri-former Predictive Thermometer is a medical device that received FDA 510(k) clearance on 2017-10-04. The listed applicant is Rudolf Riester GmbH. The 510(k) number is K171182.

When did ri-former Predictive Thermometer receive FDA 510(k) clearance?

ri-former Predictive Thermometer received FDA 510(k) clearance on 2017-10-04, under 510(k) number K171182.

Who is the listed applicant for ri-former Predictive Thermometer?

The FDA 510(k) record lists Rudolf Riester GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ri-former Predictive Thermometer?

The FDA product code for ri-former Predictive Thermometer is FLL.

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Dispositivos Relacionados (Código: FLL)

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