510(k) K842835 ยท HOI Spectacle, Magnifying
BRILLETTE MODEL
| Applicant | Cillus Company, Inc., Novato CA, US |
| Decision | Substantially Equivalent, Nov 21, 1984 |
| Received | Jul 20, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842835
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.