WYLER SPHENOIDAL ELECTRODE— 510(k) K861031
Substantially EquivalentAd-Tech Medical Instrument Corp
FDA 510(k) clearance K861031 for WYLER SPHENOIDAL ELECTRODE, Substantially Equivalent on 1986-08-25. Applicant: Ad-Tech Medical Instrument Corp. Device class: 2.
Clearance details
- Applicant
- Ad-Tech Medical Instrument Corp
- Product code
- Code GZL
- Device class
- Class 2
- Regulation
- 21 CFR 882.1330
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Racine, WI, US
Recent devices under product code GZL
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- K041604 — MACRO-MICRO DEPTH ELECTRODE
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Data sourced from openFDA. This site is unofficial and independent of the FDA.