MODEL K7 EVALUATION DEVICE— 510(k) K003287
Substantially EquivalentMyotronics-Noromed, Inc.
FDA 510(k) clearance K003287 for MODEL K7 EVALUATION DEVICE, Substantially Equivalent on 2000-11-06. Applicant: Myotronics-Noromed, Inc..
Clearance details
- Applicant
- Myotronics-Noromed, Inc.
- Product code
- Code KZM
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Tukwila, WA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.