INTERCEPT T.E.N.S. DEVICE— 510(k) K880492
Substantially EquivalentMedical Design & Manufacturing Corp.
FDA 510(k) clearance K880492 for INTERCEPT T.E.N.S. DEVICE, Substantially Equivalent on 1988-04-18. Applicant: Medical Design & Manufacturing Corp..
Clearance details
- Applicant
- Medical Design & Manufacturing Corp.
- Product code
- Code GZJ
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Westerville, OH, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.