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FDA 510(k)

DNAP Electrode

K-Number: K152547 · 2016-03-04

ApplicantAd-Tech Medical Instrument Corporation
Decision Date2016-03-04
Product CodeGZL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DNAP Electrode is a medical device manufactured by Ad-Tech Medical Instrument Corporation. It received FDA 510(k) clearance on 2016-03-04 under approval number K152547. 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 DNAP Electrode?

DNAP Electrode is a medical device that received FDA 510(k) clearance on 2016-03-04. It is manufactured by Ad-Tech Medical Instrument Corporation. The 510(k) number is K152547.

When was DNAP Electrode approved by the FDA?

DNAP Electrode received FDA 510(k) clearance on 2016-03-04, under approval number K152547.

What company makes DNAP Electrode?

DNAP Electrode is manufactured by Ad-Tech Medical Instrument Corporation.

What is the FDA product code for DNAP Electrode?

The FDA product code for DNAP Electrode is GZL.

Other Devices by Ad-Tech Medical Instrument Corporation

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Related Devices (Code: GZL)

K151790PMT Platinum Depthalon Depth ElectrodePmt Corporation K171581Neuro Omega SystemAlpha Omega Engineering , Ltd. K170959DIXI Medical Microdeep Depth ElectrodeDixi Medical K162459AccuPoint ElectrodeMicroprobes For Life Science, Inc. Dba Neuron K163355Depth Electrodes, Foramen Ovale Depth Eletrodes, Marco-Micro Depth Electrodes, Spencer Probe Depth ElectrodesAd-Tech Medical Instrument Corporation K183123microTargeting Guideline 4000 5.0 SystemFHC, Inc.

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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