FDA 510(k)

ZOMED MODEL 500 ELECTROSURGICAL GENERATOR MODEL 200 ELECTROSURGICAL PROBE

K-Number: K952072 · 1995-10-04

Decision Date1995-10-04

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ZOMED MODEL 500 ELECTROSURGICAL GENERATOR MODEL 200 ELECTROSURGICAL PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Zomed Intl.. It received FDA 510(k) clearance on 1995-10-04 under 510(k) number K952072. 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 ZOMED MODEL 500 ELECTROSURGICAL GENERATOR MODEL 200 ELECTROSURGICAL PROBE?

ZOMED MODEL 500 ELECTROSURGICAL GENERATOR MODEL 200 ELECTROSURGICAL PROBE is a medical device that received FDA 510(k) clearance on 1995-10-04. The listed applicant is Zomed Intl.. The 510(k) number is K952072.

When did ZOMED MODEL 500 ELECTROSURGICAL GENERATOR MODEL 200 ELECTROSURGICAL PROBE receive FDA 510(k) clearance?

ZOMED MODEL 500 ELECTROSURGICAL GENERATOR MODEL 200 ELECTROSURGICAL PROBE received FDA 510(k) clearance on 1995-10-04, under 510(k) number K952072.

Who is the listed applicant for ZOMED MODEL 500 ELECTROSURGICAL GENERATOR MODEL 200 ELECTROSURGICAL PROBE?

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

What is the FDA product code for ZOMED MODEL 500 ELECTROSURGICAL GENERATOR MODEL 200 ELECTROSURGICAL PROBE?

The FDA product code for ZOMED MODEL 500 ELECTROSURGICAL GENERATOR MODEL 200 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.