AD-TECH SUB DURAL ELECTRODEDS— 510(k) K923803
Substantially EquivalentAd-Tech Medical Instrument Corp
FDA 510(k) clearance K923803 for AD-TECH SUB DURAL ELECTRODEDS, Substantially Equivalent on 1992-10-23. Applicant: Ad-Tech Medical Instrument Corp. Device class: 2.
Clearance details
- Applicant
- Ad-Tech Medical Instrument Corp
- Product code
- Code GYC
- Device class
- Class 2
- Regulation
- 21 CFR 882.1310
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Racine, WI, US
Recent devices under product code GYC
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More clearances from Ad-Tech Medical Instrument Corp
view all- K112094 — BRAIN BIOPSY NEEDLE
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- K053358 — DEPTH ELECTRODE, FORAMEN OVALE DEPTH ELECTRODES, WYLER SPHENOIDAL DEPTH ELECTRODES
- K041604 — MACRO-MICRO DEPTH ELECTRODE
- K990788 — AD-TECH'S FORAMEN OVALE ELECTRODE
Data sourced from openFDA. This site is unofficial and independent of the FDA.