FDA 510(k)

BOVIE IDS-300 HIGH FREQUENCY ELECTROSURGICAL GENERATOR

K-Number: K022856 · 2003-02-10

Decision Date2003-02-10

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

BOVIE IDS-300 HIGH FREQUENCY ELECTROSURGICAL GENERATOR 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 2003-02-10 under 510(k) number K022856. 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 BOVIE IDS-300 HIGH FREQUENCY ELECTROSURGICAL GENERATOR?

BOVIE IDS-300 HIGH FREQUENCY ELECTROSURGICAL GENERATOR is a medical device that received FDA 510(k) clearance on 2003-02-10. The listed applicant is Aaron Medical Industries. The 510(k) number is K022856.

When did BOVIE IDS-300 HIGH FREQUENCY ELECTROSURGICAL GENERATOR receive FDA 510(k) clearance?

BOVIE IDS-300 HIGH FREQUENCY ELECTROSURGICAL GENERATOR received FDA 510(k) clearance on 2003-02-10, under 510(k) number K022856.

Who is the listed applicant for BOVIE IDS-300 HIGH FREQUENCY ELECTROSURGICAL GENERATOR?

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 BOVIE IDS-300 HIGH FREQUENCY ELECTROSURGICAL GENERATOR?

The FDA product code for BOVIE IDS-300 HIGH FREQUENCY ELECTROSURGICAL GENERATOR is GEI.

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Other records listing Aaron Medical Industries as applicant

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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.