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FDA 510(k)

Perforated Baskets

K-Number: K231291 · 2024-06-03

Decision Date2024-06-03
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

What is the Perforated Baskets?

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

When was Perforated Baskets approved by the FDA?

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

What company makes Perforated Baskets?

Perforated Baskets is manufactured by Richard Wolf Medical Instruments Corporation.

What is the FDA product code for Perforated Baskets?

The FDA product code for Perforated Baskets is KCT.

Other Devices by Richard Wolf Medical Instruments Corporation

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Related Devices (Code: KCT)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.