510(k) K861684 ยท HQG Lens, Spectacle, Non-Custom (Prescription)
SEIKO P-2 & SEIKO P-3 (SPECTACLE LENS)
| Applicant | Seiko Optical Products of America, Inc., Mahwah NJ, US |
| Decision | Substantially Equivalent, Jun 9, 1986 |
| Received | May 2, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861684
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.