TENZCARE DUAL-CHANNEL STIMULATOR— 510(k) K800758
Substantially Equivalent3M Company
FDA 510(k) clearance K800758 for TENZCARE DUAL-CHANNEL STIMULATOR, Substantially Equivalent on 1980-04-10. Applicant: 3M Company.
Clearance details
- Applicant
- 3M Company
- Product code
- Code GZJ
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- White City, OR, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.