510(k) K131783 ยท LRX Case, Contact Lens
POLAROID CONTACTSPOD
| Applicant | Viopti, Ltd., Dumbarton, GB |
| Decision | Substantially Equivalent, Feb 21, 2014 |
| Received | Jun 17, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131783
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.