Ultralite
FDA Regulatory Profile
Ultralite appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 30, 1991.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K910091 | ULTRALITE PANELITE | May 30, 1991 |
| K861963 | ULTRALITE HF1236 HAND AND FOOT SYSTEM | June 25, 1986 |
| K820492 | SPECTRA305 | March 31, 1982 |
| K827123 | SPECTRA (ULTRAVIOLET PRODUCTS) | March 5, 1982 |
| K820280 | SPECTRA 305/350 | March 5, 1982 |
| K761179 | PSORALITE | May 3, 1977 |