510(k) K840660 ยท HNY Cystotome
POSTERIOR CAPSULOTOMY CYSTITOME
| Applicant | Sharpoint, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 16, 1984 |
| Received | Feb 15, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840660
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.