OMNIPROBE ELECTRICAL NERVE STIMULATOR— 510(k) K831147
Substantially EquivalentOmni Intl., Inc.
FDA 510(k) clearance K831147 for OMNIPROBE ELECTRICAL NERVE STIMULATOR, Substantially Equivalent on 1983-07-18. Applicant: Omni Intl., Inc.. Device class: 2.
Clearance details
- Applicant
- Omni Intl., Inc.
- Product code
- Code GZJ
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
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