Perforated Baskets
K-Number: K231291 · 2024-06-03
Device Summary
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
Related Devices (Code: KCT)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.