510(k) K081382 ยท KYB Lens, Guide, Intraocular
DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786
| Applicant | Duckworth & Kent, Ltd., Baldock, Hertfordshire, GB |
| Decision | Substantially Equivalent, Oct 23, 2008 |
| Received | May 16, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081382
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.