FDA 510(k)

ARIEL RADIO FREQUENCY (RF) ELECTROSURGICAL CONTROL MODULE AND ACCESSORIES

K-Number: K013730 · 2002-02-06

Decision Date2002-02-06

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ARIEL RADIO FREQUENCY (RF) ELECTROSURGICAL CONTROL MODULE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Novasys Medical, Inc.. It received FDA 510(k) clearance on 2002-02-06 under 510(k) number K013730. 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 ARIEL RADIO FREQUENCY (RF) ELECTROSURGICAL CONTROL MODULE AND ACCESSORIES?

ARIEL RADIO FREQUENCY (RF) ELECTROSURGICAL CONTROL MODULE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 2002-02-06. The listed applicant is Novasys Medical, Inc.. The 510(k) number is K013730.

When did ARIEL RADIO FREQUENCY (RF) ELECTROSURGICAL CONTROL MODULE AND ACCESSORIES receive FDA 510(k) clearance?

ARIEL RADIO FREQUENCY (RF) ELECTROSURGICAL CONTROL MODULE AND ACCESSORIES received FDA 510(k) clearance on 2002-02-06, under 510(k) number K013730.

Who is the listed applicant for ARIEL RADIO FREQUENCY (RF) ELECTROSURGICAL CONTROL MODULE AND ACCESSORIES?

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

What is the FDA product code for ARIEL RADIO FREQUENCY (RF) ELECTROSURGICAL CONTROL MODULE AND ACCESSORIES?

The FDA product code for ARIEL RADIO FREQUENCY (RF) ELECTROSURGICAL CONTROL MODULE AND ACCESSORIES is GEI.

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Other records listing Novasys Medical, Inc. 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.