MA-300 ELECTROMYOGRAPHY SYSTEM— 510(k) K000220
Substantially EquivalentMotion Lab Systems, Inc.
FDA 510(k) clearance K000220 for MA-300 ELECTROMYOGRAPHY SYSTEM, Substantially Equivalent on 2000-02-24. Applicant: Motion Lab Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Motion Lab Systems, Inc.
- Product code
- Code IKN
- Device class
- Class 2
- Regulation
- 21 CFR 890.1375
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Baton Rouge, LA, US
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