REHASTIM & REHAMOVE— 510(k) K073237
Substantially EquivalentHasomed GmbH
FDA 510(k) clearance K073237 for REHASTIM & REHAMOVE, Substantially Equivalent on 2007-12-27. Applicant: Hasomed GmbH. Device class: 2.
Clearance details
- Applicant
- Hasomed GmbH
- Product code
- Code GZI
- Device class
- Class 2
- Regulation
- 21 CFR 882.5810
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Magdeburg, DE
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