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FDA 510(k)

AARON 900 HIGH FREQUENCY DESSICCATOR/HANDPIECE

K-Number: K000961 · 2000-04-19

ApplicantAaron Medical Industries
Decision Date2000-04-19
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AARON 900 HIGH FREQUENCY DESSICCATOR/HANDPIECE 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 2000-04-19 under 510(k) number K000961. 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 900 HIGH FREQUENCY DESSICCATOR/HANDPIECE?

AARON 900 HIGH FREQUENCY DESSICCATOR/HANDPIECE is a medical device that received FDA 510(k) clearance on 2000-04-19. The listed applicant is Aaron Medical Industries. The 510(k) number is K000961.

When did AARON 900 HIGH FREQUENCY DESSICCATOR/HANDPIECE receive FDA 510(k) clearance?

AARON 900 HIGH FREQUENCY DESSICCATOR/HANDPIECE received FDA 510(k) clearance on 2000-04-19, under 510(k) number K000961.

Who is the listed applicant for AARON 900 HIGH FREQUENCY DESSICCATOR/HANDPIECE?

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 900 HIGH FREQUENCY DESSICCATOR/HANDPIECE?

The FDA product code for AARON 900 HIGH FREQUENCY DESSICCATOR/HANDPIECE is GEI.

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Other records listing Aaron Medical Industries as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K062337MODULAR LAPAROSCOPY ACCESSORIES, HANDLE; SISSORS (STRAIGHT AND CURVED); GRASPER (AGGRESSIVE, ALLIS, ATAUMATIC; DISSECTORK061307BOVIE INAFLASH SUTURE REMOVER HANDLE,CHARGER,HANDLE AND CHARGER,KIT,BATTERY PACKK060117BOVIE BUTTON REMOTE HAND SWITCHK022856BOVIE IDS-300 HIGH FREQUENCY ELECTROSURGICAL GENERATORK021817AARON A950 HIGH FREQUENCY ELECTROSURGICAL GENERATOR, AARON A950 ELECTROSURGICAL GENERATOR, 240VK020579AARON ARTHROSCOPY ELECTRODE, CATALOG NUMBERS AR00, AR01, AR02, AND AR03

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Related Devices (Code: GEI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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