KGLClass II
Cabinet, Phototherapy (Puva)
21 CFR 878.4630 / General, Plastic Surgery
KGL is the FDA product code for Cabinet, Phototherapy (Puva), a class II device type, regulated under 21 CFR 878.4630. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and no recalls.
Classification record
- Product code
- KGL
- Device name
- Cabinet, Phototherapy (Puva)
- Regulation
- 21 CFR 878.4630
- Device class
- Class II
- Review panel
- General, Plastic Surgery
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- Yes
- Ingested clearances
- 8
- Ingested recalls
- 0
Clearances, product code KGL
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1976 | 1 |
| 1979 | 2 |
| 1981 | 2 |
| 1982 | 1 |
| 1984 | 1 |
| 1985 | 1 |
Applicants with the most clearances
Product code KGL| Applicant | Clearances |
|---|---|
| Paul B. Elder Co. | 3 |
| Dermatron Corp. | 1 |
| National Biological Corp. | 1 |
| Sylvania Lighting Products | 1 |
| Ultralite | 1 |
| Waldmann Lighting | 1 |
Companies listing this code with FDA
Companies whose registered establishments list this codeNo registered establishment in MDM’s records lists product code KGL.
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