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FDA 510(k)

Single Use Electrosurgical Snare SD-400

K-Number: K172734 · 2017-12-07

ApplicantOlympus Medical Systems Corp.
Decision Date2017-12-07
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Single Use Electrosurgical Snare SD-400 is a medical device manufactured by Olympus Medical Systems Corp.. It received FDA 510(k) clearance on 2017-12-07 under approval number K172734. The device is classified under product code FDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Single Use Electrosurgical Snare SD-400?

Single Use Electrosurgical Snare SD-400 is a medical device that received FDA 510(k) clearance on 2017-12-07. It is manufactured by Olympus Medical Systems Corp.. The 510(k) number is K172734.

When was Single Use Electrosurgical Snare SD-400 approved by the FDA?

Single Use Electrosurgical Snare SD-400 received FDA 510(k) clearance on 2017-12-07, under approval number K172734.

What company makes Single Use Electrosurgical Snare SD-400?

Single Use Electrosurgical Snare SD-400 is manufactured by Olympus Medical Systems Corp..

What is the FDA product code for Single Use Electrosurgical Snare SD-400?

The FDA product code for Single Use Electrosurgical Snare SD-400 is FDI.

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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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