FDA 510(k)

HAD1717MC

K-번호: K200018 · 2020-01-31

신청자H&Abyz

결정일2020-01-31

제품 코드MQB

자문 위원회RA

결정Substantially Equivalent

기기 요약

HAD1717MC is the device name listed in this FDA 510(k) record. The listed applicant is H&Abyz. It received FDA 510(k) clearance on 2020-01-31 under 510(k) number K200018. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the HAD1717MC?

HAD1717MC is a medical device that received FDA 510(k) clearance on 2020-01-31. The listed applicant is H&Abyz. The 510(k) number is K200018.

When did HAD1717MC receive FDA 510(k) clearance?

HAD1717MC received FDA 510(k) clearance on 2020-01-31, under 510(k) number K200018.

Who is the listed applicant for HAD1717MC?

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

What is the FDA product code for HAD1717MC?

The FDA product code for HAD1717MC is MQB.

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기기 요약

자주 묻는 질문

관련 기기 (코드: MQB)

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