510(k) K012698 ยท NKX Needle, Phacoemulsification, Reprocessed
VANGUARD REPROCESSED PHACOEMULSIFICATION
| Applicant | Vanguard Medical Concepts, Inc., Lakeland FL, US |
| Decision | Substantially Equivalent, Nov 9, 2001 |
| Received | Aug 14, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012698
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.