SPECTRA (ULTRAVIOLET PRODUCTS)
| Applicant | Ultralite, Wheatridge CO, US |
| Decision | Substantially Equivalent, Mar 5, 1982 |
| Received | Feb 2, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K827123
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.