# Ultralite

- Location (FDA's records): Walker, MI
- FDA decisions: 6 (1977–1991): 6 510(k) clearances
- Product codes: FTC (3), KGL (1), IOB (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K910091: Ultralite Panelite (May 30, 1991)
- K861963: Ultralite HF1236 Hand and Foot System (Jun 25, 1986)
- K820492: SPECTRA305 (Mar 31, 1982)
- K827123: Spectra (Ultraviolet Products) (Mar 5, 1982)
- K820280: Spectra 305/350 (Mar 5, 1982)
- K761179: Psoralite (May 3, 1977)

Source page: https://510kreport.com/company/ultralite