AD-TECH EPIDURAL PEG ELECTRODE— 510(k) K912760
Substantially EquivalentAd-Tech Medical Instrument Corp
FDA 510(k) clearance K912760 for AD-TECH EPIDURAL PEG ELECTRODE, Substantially Equivalent on 1992-01-15. 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
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Data sourced from openFDA. This site is unofficial and independent of the FDA.