FDA 510(k)

하이포더밀 시립스 & 나이프

K-번호: K222925 · 2023-07-18

결정일2023-07-18

제품 코드FMF

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

결정Substantially Equivalent

기기 요약

Hypodermic Syringes & Needle is the device name listed in this FDA 510(k) record. The listed applicant is Lifelong Meditech Private Limited. It received FDA 510(k) clearance on 2023-07-18 under 510(k) number K222925. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Hypodermic Syringes & Needle?

Hypodermic Syringes & Needle is a medical device that received FDA 510(k) clearance on 2023-07-18. The listed applicant is Lifelong Meditech Private Limited. The 510(k) number is K222925.

When did Hypodermic Syringes & Needle receive FDA 510(k) clearance?

Hypodermic Syringes & Needle received FDA 510(k) clearance on 2023-07-18, under 510(k) number K222925.

Who is the listed applicant for Hypodermic Syringes & Needle?

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

What is the FDA product code for Hypodermic Syringes & Needle?

The FDA product code for Hypodermic Syringes & Needle is FMF.

Lifelong Meditech Private Limited를 신청인으로 등재한 기타 기록

K210103SAFETYWAY, LIFELONG 프리미엄, LIFELONG 매트릭스

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