FDA 510(k)

AARON 2100 HIGH FREQUENCY ELECTROSURGICAL GENERATOR

K-Number: K001382 · 2000-06-27

Decision Date2000-06-27

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

AARON 2100 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 2000-06-27 under 510(k) number K001382. 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 2100 HIGH FREQUENCY ELECTROSURGICAL GENERATOR?

AARON 2100 HIGH FREQUENCY ELECTROSURGICAL GENERATOR is a medical device that received FDA 510(k) clearance on 2000-06-27. The listed applicant is Aaron Medical Industries. The 510(k) number is K001382.

When did AARON 2100 HIGH FREQUENCY ELECTROSURGICAL GENERATOR receive FDA 510(k) clearance?

AARON 2100 HIGH FREQUENCY ELECTROSURGICAL GENERATOR received FDA 510(k) clearance on 2000-06-27, under 510(k) number K001382.

Who is the listed applicant for AARON 2100 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 AARON 2100 HIGH FREQUENCY ELECTROSURGICAL GENERATOR?

The FDA product code for AARON 2100 HIGH FREQUENCY ELECTROSURGICAL GENERATOR is GEI.

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Other records listing Aaron Medical Industries as applicant

K062337MODULAR LAPAROSCOPY ACCESSORIES, HANDLE; SISSORS (STRAIGHT AND CURVED); GRASPER (AGGRESSIVE, ALLIS, ATAUMATIC; DISSECTOR K061307BOVIE INAFLASH SUTURE REMOVER HANDLE,CHARGER,HANDLE AND CHARGER,KIT,BATTERY PACK K060117BOVIE BUTTON REMOTE HAND SWITCH K022856BOVIE IDS-300 HIGH FREQUENCY ELECTROSURGICAL GENERATOR K021817AARON A950 HIGH FREQUENCY ELECTROSURGICAL GENERATOR, AARON A950 ELECTROSURGICAL GENERATOR, 240V K020579AARON ARTHROSCOPY ELECTRODE, CATALOG NUMBERS AR00, AR01, AR02, AND AR03

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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.