CLEO TL80W PROFESSIONAL CLEO TL80W PROFESSIONAL R, CLEO TL100 W PROFESSIONAL— 510(k) K940672
Substantially EquivalentPhilips Lighting Co.
FDA 510(k) clearance K940672 for CLEO TL80W PROFESSIONAL CLEO TL80W PROFESSIONAL R, CLEO TL100 W PROFESSIONAL, Substantially Equivalent on 1994-03-18. Applicant: Philips Lighting Co.. Device class: 2.
Clearance details
- Applicant
- Philips Lighting Co.
- Product code
- Code LEJ
- Device class
- Class 2
- Regulation
- 21 CFR 878.4635
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Somerset, NJ, US
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