REUSABLE CUTANEOUS ELECTRODE— 510(k) K121483
Substantially EquivalentAmpcare, LLC
FDA 510(k) clearance K121483 for REUSABLE CUTANEOUS ELECTRODE, Substantially Equivalent on 2012-10-15. Applicant: Ampcare, LLC. Device class: 2.
Clearance details
- Applicant
- Ampcare, LLC
- Product code
- Code GXY
- Device class
- Class 2
- Regulation
- 21 CFR 882.1320
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Richardson, TX, US
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More clearances from Ampcare, LLC
view allData sourced from openFDA. This site is unofficial and independent of the FDA.