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FDA 510(k)

AARON 800 HIGH FREQUENCY DESICCATOR/HANDPIECE

K-Number: K955681 · 1996-02-08

ApplicantGeiger Instrument Co., Inc.
Decision Date1996-02-08
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AARON 800 HIGH FREQUENCY DESICCATOR/HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Geiger Instrument Co., Inc.. It received FDA 510(k) clearance on 1996-02-08 under 510(k) number K955681. 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 800 HIGH FREQUENCY DESICCATOR/HANDPIECE?

AARON 800 HIGH FREQUENCY DESICCATOR/HANDPIECE is a medical device that received FDA 510(k) clearance on 1996-02-08. The listed applicant is Geiger Instrument Co., Inc.. The 510(k) number is K955681.

When did AARON 800 HIGH FREQUENCY DESICCATOR/HANDPIECE receive FDA 510(k) clearance?

AARON 800 HIGH FREQUENCY DESICCATOR/HANDPIECE received FDA 510(k) clearance on 1996-02-08, under 510(k) number K955681.

Who is the listed applicant for AARON 800 HIGH FREQUENCY DESICCATOR/HANDPIECE?

The FDA 510(k) record lists Geiger Instrument Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AARON 800 HIGH FREQUENCY DESICCATOR/HANDPIECE?

The FDA product code for AARON 800 HIGH FREQUENCY DESICCATOR/HANDPIECE is GEI.

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Official Source

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