KGL — Cabinet, Phototherapy (Puva) Class II
FDA Device Classification
Classification Details
- Product Code
- KGL
- Device Class
- Class II
- Regulation Number
- 878.4630
- Submission Type
- Review Panel
- SU
- Medical Specialty
- General, Plastic Surgery
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
| K852575 | sylvania lighting products | WALDMANN F85/100W PUVA | August 16, 1985 |
| K841795 | waldmann lighting | UV 8001K, PUVA 800, PUVA 180/200 1000 | August 30, 1984 |
| K820280 | ultralite | SPECTRA 305/350 | March 5, 1982 |
| K810668 | national biological | HO-B-LITE VI UNIT | April 23, 1981 |
| K810358 | paul b. elder | PHOTOTHERAPY LIGHT CHAMBER | March 20, 1981 |
| K791977 | paul b. elder | PSORALITE MARK I | December 28, 1979 |
| K791116 | paul b. elder | PSORALITE SERIES 30,000 | September 4, 1979 |
| K761094 | dermatron | UVA PHOTOTHERAPY SYSTEM | December 2, 1976 |