FDA 510(k)

Single Use Retrieval Basket V FG-V421PR/V422PR/V431P/V432P

Número K: K243807 · 2025-03-18

Data da decisão2025-03-18

Código do produtoLQR

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Single Use Retrieval Basket V FG-V421PR/V422PR/V431P/V432P is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Medical Systems Corp.. It received FDA 510(k) clearance on 2025-03-18 under 510(k) number K243807. The device is classified under product code LQR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Single Use Retrieval Basket V FG-V421PR/V422PR/V431P/V432P?

Single Use Retrieval Basket V FG-V421PR/V422PR/V431P/V432P is a medical device that received FDA 510(k) clearance on 2025-03-18. The listed applicant is Olympus Medical Systems Corp.. The 510(k) number is K243807.

When did Single Use Retrieval Basket V FG-V421PR/V422PR/V431P/V432P receive FDA 510(k) clearance?

Single Use Retrieval Basket V FG-V421PR/V422PR/V431P/V432P received FDA 510(k) clearance on 2025-03-18, under 510(k) number K243807.

Who is the listed applicant for Single Use Retrieval Basket V FG-V421PR/V422PR/V431P/V432P?

The FDA 510(k) record lists Olympus Medical Systems Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Single Use Retrieval Basket V FG-V421PR/V422PR/V431P/V432P?

The FDA product code for Single Use Retrieval Basket V FG-V421PR/V422PR/V431P/V432P is LQR.

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Fonte oficial

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