FDA 510(k)

무균 자연 라텍스 수술 장갑 (Powdered Free Sterile Natural Rubber Latex Surgical Gloves)

K-번호: K230832 · 2023-08-16

신청자The Egyptian Company For Medical & Electronic Industries

결정일2023-08-16

제품 코드KGO

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

결정대체적으로 동일

기기 요약

Powdered Free Sterile Natural Rubber Latex Surgical Gloves is the device name listed in this FDA 510(k) record. The listed applicant is The Egyptian Company For Medical & Electronic Industries. It received FDA 510(k) clearance on 2023-08-16 under 510(k) number K230832. 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 Powdered Free Sterile Natural Rubber Latex Surgical Gloves?

Powdered Free Sterile Natural Rubber Latex Surgical Gloves is a medical device that received FDA 510(k) clearance on 2023-08-16. The listed applicant is The Egyptian Company For Medical & Electronic Industries. The 510(k) number is K230832.

When did Powdered Free Sterile Natural Rubber Latex Surgical Gloves receive FDA 510(k) clearance?

Powdered Free Sterile Natural Rubber Latex Surgical Gloves received FDA 510(k) clearance on 2023-08-16, under 510(k) number K230832.

Who is the listed applicant for Powdered Free Sterile Natural Rubber Latex Surgical Gloves?

The FDA 510(k) record lists The Egyptian Company For Medical & Electronic Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Powdered Free Sterile Natural Rubber Latex Surgical Gloves?

The FDA product code for Powdered Free Sterile Natural Rubber Latex Surgical Gloves is KGO.

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FDA 데이터베이스에서 보기 →

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

무균 자연 라텍스 수술 장갑 (Powdered Free Sterile Natural Rubber Latex Surgical Gloves)

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: KGO)

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