510(k) K120996 ยท HQD Lens, Contact (Other Material) - Daily
FLUOROPERM 30 PARAGON HDS FLUOROPERM 60 PARAGON HDS 100 FLUOROPERM 92 FLUOROPERM 151 PARAGON THIN
| Applicant | Paragon Vision Sciences, Mesa AZ, US |
| Decision | Substantially Equivalent, Jun 28, 2012 |
| Received | Apr 2, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120996
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.