FDA 510(k)

SERFAS 90-S Electrosurgical Probe

K-Number: K160050 · 2016-05-03

Decision Date2016-05-03

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SERFAS 90-S Electrosurgical Probe is a medical device manufactured by Stryker Corporation. It received FDA 510(k) clearance on 2016-05-03 under approval number K160050. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERFAS 90-S Electrosurgical Probe?

SERFAS 90-S Electrosurgical Probe is a medical device that received FDA 510(k) clearance on 2016-05-03. It is manufactured by Stryker Corporation. The 510(k) number is K160050.

When was SERFAS 90-S Electrosurgical Probe approved by the FDA?

SERFAS 90-S Electrosurgical Probe received FDA 510(k) clearance on 2016-05-03, under approval number K160050.

What company makes SERFAS 90-S Electrosurgical Probe?

SERFAS 90-S Electrosurgical Probe is manufactured by Stryker Corporation.

What is the FDA product code for SERFAS 90-S Electrosurgical Probe?

The FDA product code for SERFAS 90-S Electrosurgical Probe is GEI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.