FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CLEO TL80W PROFESSIONAL CLEO TL80W PROFESSIONAL R, CLEO TL100 W PROFESSIONAL
K Number: K940672
·
Decision Mar 18, 1994
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
80
Applicant Total
6
Review Days
30
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Basic Information
- Device Name
- CLEO TL80W PROFESSIONAL CLEO TL80W PROFESSIONAL R, CLEO TL100 W PROFESSIONAL
- K Number
- K940672
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4635
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Philips Lighting Co.
- Date Received
- February 16, 1994
- Decision Date
- March 18, 1994
- Product Code
- LEJ
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| LEJ | Booth, Sun Tan | FDA class 2 | General, Plastic Surgery |
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Other Clearances by Philips Lighting Co.
| K Number | Device Name | ||
|---|---|---|---|
| K021514 | PHILIPS PLS9W/12/2P UVB | May 16, 2002 | Substantially Equivalent |
| K021092 | PHILIPS TL 20W/01RS UV-B, PHILIPS PL-S 9W/01/2P UV, AND PHILIPS PL-L 36W/01/4P UV-B | May 16, 2002 | Substantially Equivalent |
| K935840 | TL 20W/12/RS & TL 40W/12/RS | Feb 24, 1994 | Substantially Equivalent |
| K922963 | TL100W/12 | Sep 2, 1992 | Substantially Equivalent |
| K910767 | TL100W/01 UVB LAMP | May 23, 1991 | Substantially Equivalent |