FDA 510(k)

TrueView 100 Pro

K-번호: K202713 · 2020-11-18

결정일2020-11-18

제품 코드MWP

자문 위원회RA

결정Substantially Equivalent

기기 요약

TrueView 100 Pro is the device name listed in this FDA 510(k) record. The listed applicant is Compai Healthcare (Shenzhen) Co.,Ltd. It received FDA 510(k) clearance on 2020-11-18 under 510(k) number K202713. The device is classified under product code MWP. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the TrueView 100 Pro?

TrueView 100 Pro is a medical device that received FDA 510(k) clearance on 2020-11-18. The listed applicant is Compai Healthcare (Shenzhen) Co.,Ltd. The 510(k) number is K202713.

When did TrueView 100 Pro receive FDA 510(k) clearance?

TrueView 100 Pro received FDA 510(k) clearance on 2020-11-18, under 510(k) number K202713.

Who is the listed applicant for TrueView 100 Pro?

The FDA 510(k) record lists Compai Healthcare (Shenzhen) Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TrueView 100 Pro?

The FDA product code for TrueView 100 Pro is MWP.

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TrueView 100 Pro

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: MWP)

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