LUMISCOPE TENS MODEL 2000T OR APCC 3001 OR PAIN RE— 510(k) K880452
Substantially EquivalentLumiscope Co., Inc.
FDA 510(k) clearance K880452 for LUMISCOPE TENS MODEL 2000T OR APCC 3001 OR PAIN RE, Substantially Equivalent on 1988-03-24. Applicant: Lumiscope Co., Inc..
Clearance details
- Applicant
- Lumiscope Co., Inc.
- Product code
- Code GZJ
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Edison, NJ, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.