FDA 510(k)

CUEVA CRANIAL NERVE ELECTRODE

K-Number: K944061 · 1995-01-20

ApplicantAd-Tech Medical Instrument Corp

Decision Date1995-01-20

Product CodeGZL

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

CUEVA CRANIAL NERVE ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Ad-Tech Medical Instrument Corp. It received FDA 510(k) clearance on 1995-01-20 under 510(k) number K944061. The device is classified under product code GZL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUEVA CRANIAL NERVE ELECTRODE?

CUEVA CRANIAL NERVE ELECTRODE is a medical device that received FDA 510(k) clearance on 1995-01-20. The listed applicant is Ad-Tech Medical Instrument Corp. The 510(k) number is K944061.

When did CUEVA CRANIAL NERVE ELECTRODE receive FDA 510(k) clearance?

CUEVA CRANIAL NERVE ELECTRODE received FDA 510(k) clearance on 1995-01-20, under 510(k) number K944061.

Who is the listed applicant for CUEVA CRANIAL NERVE ELECTRODE?

The FDA 510(k) record lists Ad-Tech Medical Instrument Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CUEVA CRANIAL NERVE ELECTRODE?

The FDA product code for CUEVA CRANIAL NERVE ELECTRODE is GZL.

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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.