TENZCARE STIMULATOR 6890— 510(k) K891992
Substantially Equivalent3M Company
FDA 510(k) clearance K891992 for TENZCARE STIMULATOR 6890, Substantially Equivalent on 1989-10-12. Applicant: 3M Company. Device class: 2.
Clearance details
- Applicant
- 3M Company
- Product code
- Code GZJ
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cottae Grove, MN, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.