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FDA 510(k)

SERFAS 90-S Electrosurgical Probe

K-Number: K160050 · 2016-05-03

ApplicantStryker Corporation
Decision Date2016-05-03
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SERFAS 90-S Electrosurgical Probe is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corporation. It received FDA 510(k) clearance on 2016-05-03 under 510(k) 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. The listed applicant is Stryker Corporation. The 510(k) number is K160050.

When did SERFAS 90-S Electrosurgical Probe receive FDA 510(k) clearance?

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

Who is the listed applicant for SERFAS 90-S Electrosurgical Probe?

The FDA 510(k) record lists Stryker Corporation as the applicant. This does not by itself establish the device manufacturer.

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

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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