FDA 510(k)

NERVE LOCATOR/STIMULATOR

K-Number: K905045 · 1991-03-15

Decision Date1991-03-15

Product CodeETN

Advisory CommitteeEN

DecisionSubstantially Equivalent

Device Summary

NERVE LOCATOR/STIMULATOR 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 1991-03-15 under 510(k) number K905045. The device is classified under product code ETN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NERVE LOCATOR/STIMULATOR?

NERVE LOCATOR/STIMULATOR is a medical device that received FDA 510(k) clearance on 1991-03-15. The listed applicant is Aaron Medical Industries. The 510(k) number is K905045.

When did NERVE LOCATOR/STIMULATOR receive FDA 510(k) clearance?

NERVE LOCATOR/STIMULATOR received FDA 510(k) clearance on 1991-03-15, under 510(k) number K905045.

Who is the listed applicant for NERVE LOCATOR/STIMULATOR?

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 NERVE LOCATOR/STIMULATOR?

The FDA product code for NERVE LOCATOR/STIMULATOR is ETN.

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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.