KINESIA— 510(k) K063872
Substantially EquivalentCleveland Medical Devices, Inc.
FDA 510(k) clearance K063872 for KINESIA, Substantially Equivalent on 2007-04-06. Applicant: Cleveland Medical Devices, Inc.. Device class: 2.
Clearance details
- Applicant
- Cleveland Medical Devices, Inc.
- Product code
- Code GYD
- Device class
- Class 2
- Regulation
- 21 CFR 882.1950
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cleveland, OH, US
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