FDA 510(k)

Aygün Sterilization Container Systems

K-번호: K233222 · 2023-12-12

결정일2023-12-12

제품 코드KCT

자문 위원회HO

결정Substantially Equivalent

기기 요약

Aygün Sterilization Container Systems is the device name listed in this FDA 510(k) record. The listed applicant is Aygun Surgical Instruments Co., Inc.. It received FDA 510(k) clearance on 2023-12-12 under 510(k) number K233222. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Aygün Sterilization Container Systems?

Aygün Sterilization Container Systems is a medical device that received FDA 510(k) clearance on 2023-12-12. The listed applicant is Aygun Surgical Instruments Co., Inc.. The 510(k) number is K233222.

When did Aygün Sterilization Container Systems receive FDA 510(k) clearance?

Aygün Sterilization Container Systems received FDA 510(k) clearance on 2023-12-12, under 510(k) number K233222.

Who is the listed applicant for Aygün Sterilization Container Systems?

The FDA 510(k) record lists Aygun Surgical Instruments Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Aygün Sterilization Container Systems?

The FDA product code for Aygün Sterilization Container Systems is KCT.

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Aygün Sterilization Container Systems

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: KCT)

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