510(k) K952260 ยท HQD Lens, Contact (Other Material) - Daily
OP-2 (LOTIFOCON B) & OP-6 (LOTIFOCON C)
| Applicant | Stellar Contact Lens, Inc., Chicago IL, US |
| Decision | Substantially Equivalent, Jan 3, 1996 |
| Received | May 15, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952260
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.