FDA 510(k)

Withings Thermo (Model SCT01)

K-번호: K160544 · 2016-06-17

결정일2016-06-17

제품 코드FLL

자문 위원회의료장비 규제 텍스트 번역 HO [원문 텍스트가 제공되지 않았기 때문에 번역할 수 없습니다. 원문 텍스트를 제공해 주시면 번역을 도와드리겠습니다.]

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기기 요약

Withings Thermo (Model SCT01) is the device name listed in this FDA 510(k) record. The listed applicant is Withings. It received FDA 510(k) clearance on 2016-06-17 under 510(k) number K160544. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Withings Thermo (Model SCT01)?

Withings Thermo (Model SCT01) is a medical device that received FDA 510(k) clearance on 2016-06-17. The listed applicant is Withings. The 510(k) number is K160544.

When did Withings Thermo (Model SCT01) receive FDA 510(k) clearance?

Withings Thermo (Model SCT01) received FDA 510(k) clearance on 2016-06-17, under 510(k) number K160544.

Who is the listed applicant for Withings Thermo (Model SCT01)?

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

What is the FDA product code for Withings Thermo (Model SCT01)?

The FDA product code for Withings Thermo (Model SCT01) is FLL.

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