STIMTECH TENS ELECTRODE— 510(k) K790345
Substantially EquivalentStimulation Technology, Inc.
FDA 510(k) clearance K790345 for STIMTECH TENS ELECTRODE, Substantially Equivalent on 1979-03-21. Applicant: Stimulation Technology, Inc..
Clearance details
- Applicant
- Stimulation Technology, Inc.
- Product code
- Code GXY
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.