FDA 510(k)

정화된 비포함 실리콘 수술 의사 장갑, 피부염 가능성 낮음

K-번호: K191860 · 2020-03-31

신청자Semperit Technische Produkte Gesellchaft M.B.H.

결정일2020-03-31

제품 코드KGO

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

결정대체적으로 동일

기기 요약

Sterile Powder-Free Synthetic Rubber Surgeon’s Glove with Low Dermatitis Potential is the device name listed in this FDA 510(k) record. The listed applicant is Semperit Technische Produkte Gesellchaft M.B.H.. It received FDA 510(k) clearance on 2020-03-31 under 510(k) number K191860. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Sterile Powder-Free Synthetic Rubber Surgeon’s Glove with Low Dermatitis Potential?

Sterile Powder-Free Synthetic Rubber Surgeon’s Glove with Low Dermatitis Potential is a medical device that received FDA 510(k) clearance on 2020-03-31. The listed applicant is Semperit Technische Produkte Gesellchaft M.B.H.. The 510(k) number is K191860.

When did Sterile Powder-Free Synthetic Rubber Surgeon’s Glove with Low Dermatitis Potential receive FDA 510(k) clearance?

Sterile Powder-Free Synthetic Rubber Surgeon’s Glove with Low Dermatitis Potential received FDA 510(k) clearance on 2020-03-31, under 510(k) number K191860.

Who is the listed applicant for Sterile Powder-Free Synthetic Rubber Surgeon’s Glove with Low Dermatitis Potential?

The FDA 510(k) record lists Semperit Technische Produkte Gesellchaft M.B.H. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sterile Powder-Free Synthetic Rubber Surgeon’s Glove with Low Dermatitis Potential?

The FDA product code for Sterile Powder-Free Synthetic Rubber Surgeon’s Glove with Low Dermatitis Potential is KGO.

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FDA 데이터베이스에서 보기 →

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

정화된 비포함 실리콘 수술 의사 장갑, 피부염 가능성 낮음

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: KGO)

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