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FDA 510(k)

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

K-Number: K243807 · 2025-03-18

ApplicantOlympus Medical Systems Corp.
Decision Date2025-03-18
Product CodeLQR
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

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. It is manufactured by Olympus Medical Systems Corp.. The 510(k) number is K243807.

When was Single Use Retrieval Basket V FG-V421PR/V422PR/V431P/V432P approved by the FDA?

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

What company makes Single Use Retrieval Basket V FG-V421PR/V422PR/V431P/V432P?

Single Use Retrieval Basket V FG-V421PR/V422PR/V431P/V432P is manufactured by Olympus Medical Systems Corp..

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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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.

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