Resection Electrodes with HF cable
K-Number: K171965 · 2017-09-28
ApplicantOlympus Winter & Ibe GmbH
Decision Date2017-09-28
Product CodeFAS
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Resection Electrodes with HF cable is a medical device manufactured by Olympus Winter & Ibe GmbH. It received FDA 510(k) clearance on 2017-09-28 under approval number K171965. The device is classified under product code FAS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Resection Electrodes with HF cable?
Resection Electrodes with HF cable is a medical device that received FDA 510(k) clearance on 2017-09-28. It is manufactured by Olympus Winter & Ibe GmbH. The 510(k) number is K171965.
When was Resection Electrodes with HF cable approved by the FDA?
Resection Electrodes with HF cable received FDA 510(k) clearance on 2017-09-28, under approval number K171965.
What company makes Resection Electrodes with HF cable?
Resection Electrodes with HF cable is manufactured by Olympus Winter & Ibe GmbH.
What is the FDA product code for Resection Electrodes with HF cable?
The FDA product code for Resection Electrodes with HF cable is FAS.
Related Clinical Trials
Other Devices by Olympus Winter & Ibe GmbH
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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.