FDA 510(k)

MACRO-MICRO DEPTH ELECTRODE

K-Number: K041604 · 2004-08-16

ApplicantAd-Tech Medical Instrument Corp

Decision Date2004-08-16

Product CodeGZL

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MACRO-MICRO DEPTH 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 2004-08-16 under 510(k) number K041604. 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 MACRO-MICRO DEPTH ELECTRODE?

MACRO-MICRO DEPTH ELECTRODE is a medical device that received FDA 510(k) clearance on 2004-08-16. The listed applicant is Ad-Tech Medical Instrument Corp. The 510(k) number is K041604.

When did MACRO-MICRO DEPTH ELECTRODE receive FDA 510(k) clearance?

MACRO-MICRO DEPTH ELECTRODE received FDA 510(k) clearance on 2004-08-16, under 510(k) number K041604.

Who is the listed applicant for MACRO-MICRO DEPTH 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 MACRO-MICRO DEPTH ELECTRODE?

The FDA product code for MACRO-MICRO DEPTH 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.