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. 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.
Other records listing Richard Wolf Medical Instruments Corporation as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KCT)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.