DIGITAL EMG MONITOR MYOTRON 120— 510(k) K882266
Substantially EquivalentAts Co.
FDA 510(k) clearance K882266 for DIGITAL EMG MONITOR MYOTRON 120, Substantially Equivalent on 1988-08-15. Applicant: Ats Co..
Clearance details
- Applicant
- Ats Co.
- Product code
- Code HCC
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Riverside, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.