510(k) K022723 ยท KYB Lens, Guide, Intraocular
MASTEL 1 FOLDER IMPLANTATION SYSTEM
| Applicant | Mastel Precision, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Dec 26, 2002 |
| Received | Aug 16, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022723
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.