510(k) K160212 ยท LPL Lenses, Soft Contact, Daily Wear
ACUVUE (senofilcon C) Soft Contact Lens
| Applicant | Johnson & Johnson Vision Care, Inc., Jacksonville FL, US |
| Decision | Substantially Equivalent, Mar 28, 2016 |
| Received | Jan 29, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160212
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 6, 2021 | Johnson & Johnson Vision Care, Inc. ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear. Base Curve 8.8,
Refractive Power -1.50 Terminated |
LPL | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.