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.. Device class: 2.
Clearance details
- Applicant
- Lumiscope Co., Inc.
- 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
- Edison, NJ, US
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