FDA 510(k)

EverLift Submucosal Lifting Agent

K-번호: K191923 · 2020-06-20

결정일2020-06-20

제품 코드PLL

자문 위원회GU

결정Substantially Equivalent

기기 요약

EverLift Submucosal Lifting Agent is the device name listed in this FDA 510(k) record. The listed applicant is Gi Supply. It received FDA 510(k) clearance on 2020-06-20 under 510(k) number K191923. The device is classified under product code PLL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the EverLift Submucosal Lifting Agent?

EverLift Submucosal Lifting Agent is a medical device that received FDA 510(k) clearance on 2020-06-20. The listed applicant is Gi Supply. The 510(k) number is K191923.

When did EverLift Submucosal Lifting Agent receive FDA 510(k) clearance?

EverLift Submucosal Lifting Agent received FDA 510(k) clearance on 2020-06-20, under 510(k) number K191923.

Who is the listed applicant for EverLift Submucosal Lifting Agent?

The FDA 510(k) record lists Gi Supply as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EverLift Submucosal Lifting Agent?

The FDA product code for EverLift Submucosal Lifting Agent is PLL.

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EverLift Submucosal Lifting Agent

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: PLL)

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