MODEL MK II TENS— 510(k) K833251
Substantially EquivalentEuropean Electronic Systems, Ltd.
FDA 510(k) clearance K833251 for MODEL MK II TENS, Substantially Equivalent on 1984-03-05. Applicant: European Electronic Systems, Ltd..
Clearance details
- Applicant
- European Electronic Systems, Ltd.
- Product code
- Code GZJ
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.