KIMSTIM AURICULAR ELECTRODE— 510(k) K011691
Substantially EquivalentKim Institute For Rehabilitation Medicine, P.C.
FDA 510(k) clearance K011691 for KIMSTIM AURICULAR ELECTRODE, Substantially Equivalent on 2001-12-27. Applicant: Kim Institute For Rehabilitation Medicine, P.C.. Device class: 2.
Clearance details
- Applicant
- Kim Institute For Rehabilitation Medicine, P.C.
- 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
- Midvale, UT, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.