FDA 510(k)

Stimucel 시스템, Stimucel 제너레이터, Stimucel 트리트먼트 워ンド, Stimucel 애플리케이터

K-번호: K162721 · 2016-12-22

결정일2016-12-22

제품 코드NRB

자문 위원회SU [원문이 제공되지 않았기 때문에 번역할 수 없습니다. 원문을 제공해 주시면 번역을 도와드리겠습니다.]

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기기 요약

Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator is the device name listed in this FDA 510(k) record. The listed applicant is Alliqua Biomedical, Inc.. It received FDA 510(k) clearance on 2016-12-22 under 510(k) number K162721. The device is classified under product code NRB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator?

Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator is a medical device that received FDA 510(k) clearance on 2016-12-22. The listed applicant is Alliqua Biomedical, Inc.. The 510(k) number is K162721.

When did Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator receive FDA 510(k) clearance?

Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator received FDA 510(k) clearance on 2016-12-22, under 510(k) number K162721.

Who is the listed applicant for Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator?

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

What is the FDA product code for Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator?

The FDA product code for Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator is NRB.

Alliqua Biomedical, Inc.를 신청인으로 등재한 기타 기록

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FDA Open API에서 수집된 데이터입니다. 가장 정확하고 공인된 정보는 항상 공식 레코드를 참조하시기 바랍니다.

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