FDA Product Code
FDA Product Code KGL — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- General, Plastic Surgery
- 21 CFR Citation
- 878.4630
510(k) Clearances — 8 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K852575 | WALDMANN F85/100W PUVA | Sylvania Lighting Products | 1985-08-16 | Traditional | PDF ↗ |
| K841795 | UV 8001K, PUVA 800, PUVA 180/200 1000 | Waldmann Lighting Co. | 1984-08-30 | Traditional | PDF ↗ |
| K820280 | SPECTRA 305/350 | Ultralite | 1982-03-05 | Traditional | PDF ↗ |
| K810668 | HO-B-LITE VI UNIT | National Biological Corp. | 1981-04-23 | Traditional | PDF ↗ |
| K810358 | PHOTOTHERAPY LIGHT CHAMBER | Paul B. Elder Co. | 1981-03-20 | Traditional | PDF ↗ |
| K791977 | PSORALITE MARK I | Paul B. Elder Co. | 1979-12-28 | Traditional | PDF ↗ |
| K791116 | PSORALITE SERIES 30,000 | Paul B. Elder Co. | 1979-09-04 | Traditional | PDF ↗ |
| K761094 | UVA PHOTOTHERAPY SYSTEM | Dermatron Corp. | 1976-12-02 | Traditional | PDF ↗ |
Product code KGL · Class II · General, Plastic Surgery. Data: openFDA.