FDA 510(k)

Single Use Retrieval Nitinol Basket V

K-Number: K170811 · 2017-11-27

Decision Date2017-11-27

Product CodeLQR

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

Single Use Retrieval Nitinol Basket V is a medical device manufactured by Olympus Medical Systems Corp.. It received FDA 510(k) clearance on 2017-11-27 under approval number K170811. 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 Nitinol Basket V?

Single Use Retrieval Nitinol Basket V is a medical device that received FDA 510(k) clearance on 2017-11-27. It is manufactured by Olympus Medical Systems Corp.. The 510(k) number is K170811.

When was Single Use Retrieval Nitinol Basket V approved by the FDA?

Single Use Retrieval Nitinol Basket V received FDA 510(k) clearance on 2017-11-27, under approval number K170811.

What company makes Single Use Retrieval Nitinol Basket V?

Single Use Retrieval Nitinol Basket V is manufactured by Olympus Medical Systems Corp..

What is the FDA product code for Single Use Retrieval Nitinol Basket V?

The FDA product code for Single Use Retrieval Nitinol Basket V is LQR.

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Related Devices (Code: 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.