MS-100 MYO-SCANNER OR MS-100 EMG SCANNER— 510(k) K921919
Substantially EquivalentMyo-Tronics, Inc.
FDA 510(k) clearance K921919 for MS-100 MYO-SCANNER OR MS-100 EMG SCANNER, Substantially Equivalent on 1993-01-07. Applicant: Myo-Tronics, Inc.. Device class: 2.
Clearance details
- Applicant
- Myo-Tronics, Inc.
- Product code
- Code KZM
- Device class
- Class 2
- Regulation
- 21 CFR 890.1375
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Seattle, WA, US
Recent devices under product code KZM
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