LUMISCOPE EMS 8000— 510(k) K901849
Substantially EquivalentLumiscope Co., Inc.
FDA 510(k) clearance K901849 for LUMISCOPE EMS 8000, Substantially Equivalent on 1990-08-24. Applicant: Lumiscope Co., Inc.. Device class: 2.
Clearance details
- Applicant
- Lumiscope Co., Inc.
- Product code
- Code IPF
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Edison, NJ, US
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