SHE-LI TENS STIMULATOR MODEL SL-101 RX— 510(k) K961809
Substantially EquivalentMedi Consultants, Inc.
FDA 510(k) clearance K961809 for SHE-LI TENS STIMULATOR MODEL SL-101 RX, Substantially Equivalent on 1997-02-26. Applicant: Medi Consultants, Inc..
Clearance details
- Applicant
- Medi Consultants, Inc.
- Product code
- Code GZJ
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Paterson, NJ, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.