FDA 510(k)

AARON 1200 HIGH FREQUENCY ELECTROSURGICL GENERATOR A1200, A1200/240

K-Number: K980366 · 1998-02-27

Decision Date1998-02-27

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

AARON 1200 HIGH FREQUENCY ELECTROSURGICL GENERATOR A1200, A1200/240 is the device name listed in this FDA 510(k) record. The listed applicant is Aaron Medical Industries. It received FDA 510(k) clearance on 1998-02-27 under 510(k) number K980366. 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 AARON 1200 HIGH FREQUENCY ELECTROSURGICL GENERATOR A1200, A1200/240?

AARON 1200 HIGH FREQUENCY ELECTROSURGICL GENERATOR A1200, A1200/240 is a medical device that received FDA 510(k) clearance on 1998-02-27. The listed applicant is Aaron Medical Industries. The 510(k) number is K980366.

When did AARON 1200 HIGH FREQUENCY ELECTROSURGICL GENERATOR A1200, A1200/240 receive FDA 510(k) clearance?

AARON 1200 HIGH FREQUENCY ELECTROSURGICL GENERATOR A1200, A1200/240 received FDA 510(k) clearance on 1998-02-27, under 510(k) number K980366.

Who is the listed applicant for AARON 1200 HIGH FREQUENCY ELECTROSURGICL GENERATOR A1200, A1200/240?

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

What is the FDA product code for AARON 1200 HIGH FREQUENCY ELECTROSURGICL GENERATOR A1200, A1200/240?

The FDA product code for AARON 1200 HIGH FREQUENCY ELECTROSURGICL GENERATOR A1200, A1200/240 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.