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FDA 510(k)

AD-TECH'S DEPTH ELECTRODE

K-Number: K891920 · 1989-07-27

ApplicantAd-Tech Medical Instrument Corp
Decision Date1989-07-27
Product CodeGZL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

AD-TECH'S 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 1989-07-27 under 510(k) number K891920. 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 AD-TECH'S DEPTH ELECTRODE?

AD-TECH'S DEPTH ELECTRODE is a medical device that received FDA 510(k) clearance on 1989-07-27. The listed applicant is Ad-Tech Medical Instrument Corp. The 510(k) number is K891920.

When did AD-TECH'S DEPTH ELECTRODE receive FDA 510(k) clearance?

AD-TECH'S DEPTH ELECTRODE received FDA 510(k) clearance on 1989-07-27, under 510(k) number K891920.

Who is the listed applicant for AD-TECH'S 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 AD-TECH'S DEPTH ELECTRODE?

The FDA product code for AD-TECH'S DEPTH ELECTRODE is GZL.

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Other records listing Ad-Tech Medical Instrument Corp as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K112094BRAIN BIOPSY NEEDLEK053363DUAL-SIDED INTERHEMISPHERIC SUBDURAL ELECTRODES, GRID SUBDURAL ELECTRODES, INTRAOPERATIVE SUBDURAL ELECTRODESK053358DEPTH ELECTRODE, FORAMEN OVALE DEPTH ELECTRODES, WYLER SPHENOIDAL DEPTH ELECTRODESK041604MACRO-MICRO DEPTH ELECTRODEK990788AD-TECH'S FORAMEN OVALE ELECTRODEK992194CORTICAL MAPPING UNIT, MODEL CMU

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Related Devices (Code: GZL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253970Wovyn Depth ElectrodeSensomedical Labs, Ltd.K250363Depth Electrode (RSDE-08); Depth Electrode (RSDE-10); Depth Electrode (RSDE-12); Depth Electrode (RSDE-14); Depth Electrode (RSDE-16); Depth Electrode (RSDE-16F); Depth Electrode (RSDE-08S); Depth Electrode (RSDE-10S); Depth Electrode (RSDE-12S); Depth Electrode (RSDE-14S); Depth Electrode (RSDE-16S); Depth Electrode (RSDE-16G); Depth Electrode (RSDE-18); Depth Electrode (RSDE-18F); Depth Electrode (RSDE-18T); Depth Electrode (RSDE-20); Depth Electrode (RSDE-20F); DeptBeijing Sinovation Medical Technology Co., Ltd.K250601Neuro Omega System; NeuroSmart SystemAlpha Omega Engineering , Ltd.K223269Spencer Probe Depth ElectrodesAd-Tech Medical Instrument CorporationK223276Anchor Bolts as Accessories to Depth ElectrodesAd-Tech Medical Instrument CorporationK213170SENSOSEEG Depth ElectrodesSensomedical Labs, Ltd.

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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