FDA 510(k)

Perforated Baskets

Número K: K231291 · 2024-06-03

RequerenteRichard Wolf Medical Instruments Corporation

Data da decisão2024-06-03

Código do produtoKCT

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Perforated Baskets is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corporation. It received FDA 510(k) clearance on 2024-06-03 under 510(k) number K231291. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Perforated Baskets?

Perforated Baskets is a medical device that received FDA 510(k) clearance on 2024-06-03. The listed applicant is Richard Wolf Medical Instruments Corporation. The 510(k) number is K231291.

When did Perforated Baskets receive FDA 510(k) clearance?

Perforated Baskets received FDA 510(k) clearance on 2024-06-03, under 510(k) number K231291.

Who is the listed applicant for Perforated Baskets?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Perforated Baskets?

The FDA product code for Perforated Baskets is KCT.

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Fonte oficial

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