FDA 510(k)

LapBox Tissue Containment Removal System

Número K: K221365 · 2022-08-25

Data da decisão2022-08-25

Código do produtoGCJ

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

LapBox Tissue Containment Removal System is the device name listed in this FDA 510(k) record. The listed applicant is Ark Surgical, Ltd.. It received FDA 510(k) clearance on 2022-08-25 under 510(k) number K221365. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the LapBox Tissue Containment Removal System?

LapBox Tissue Containment Removal System is a medical device that received FDA 510(k) clearance on 2022-08-25. The listed applicant is Ark Surgical, Ltd.. The 510(k) number is K221365.

When did LapBox Tissue Containment Removal System receive FDA 510(k) clearance?

LapBox Tissue Containment Removal System received FDA 510(k) clearance on 2022-08-25, under 510(k) number K221365.

Who is the listed applicant for LapBox Tissue Containment Removal System?

The FDA 510(k) record lists Ark Surgical, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LapBox Tissue Containment Removal System?

The FDA product code for LapBox Tissue Containment Removal System is GCJ.

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