Single Use Retrieval Nitinol Basket V
K-Number: K170811 · 2017-11-27
Device Summary
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. The listed applicant is Olympus Medical Systems Corp.. The 510(k) number is K170811.
When did Single Use Retrieval Nitinol Basket V receive FDA 510(k) clearance?
Single Use Retrieval Nitinol Basket V received FDA 510(k) clearance on 2017-11-27, under 510(k) number K170811.
Who is the listed applicant for Single Use Retrieval Nitinol Basket V?
The FDA 510(k) record lists Olympus Medical Systems Corp. as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Olympus Medical Systems Corp. 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: LQR)
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.