FDA 510(k)

Disposable Dual Action Tissue Clip

Número K: K212748 · 2022-01-20

RequerenteMicro-Tech (Nanjing) Co., Ltd.

Data da decisão2022-01-20

Código do produtoPKL

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Disposable Dual Action Tissue Clip is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Tech (Nanjing) Co., Ltd.. It received FDA 510(k) clearance on 2022-01-20 under 510(k) number K212748. The device is classified under product code PKL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Disposable Dual Action Tissue Clip?

Disposable Dual Action Tissue Clip is a medical device that received FDA 510(k) clearance on 2022-01-20. The listed applicant is Micro-Tech (Nanjing) Co., Ltd.. The 510(k) number is K212748.

When did Disposable Dual Action Tissue Clip receive FDA 510(k) clearance?

Disposable Dual Action Tissue Clip received FDA 510(k) clearance on 2022-01-20, under 510(k) number K212748.

Who is the listed applicant for Disposable Dual Action Tissue Clip?

The FDA 510(k) record lists Micro-Tech (Nanjing) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Dual Action Tissue Clip?

The FDA product code for Disposable Dual Action Tissue Clip is PKL.

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Outros registros que listam Micro-Tech (Nanjing) Co., Ltd. como candidato(a)

K252492Visualized Access and Delivery Catheter; PB Digital Controller K251692Dispositivo de Resseção de Tecido Avançado K250229Dual Action Tissue Closure Device K243388Disposable Distal Cap K243471Extraction Basket K230127Biliary Plastic Stent, Biliary Plastic Stent Introducer, Biliary Plastic Stent Set, Biliary Plastic Stent Introducer/ short-wire compatible, Biliary Plastic Stent Set/ short-wire compatible

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Fonte oficial

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