510(k) K880785 ยท KDD Kit, Surgical Instrument, Disposable
SKILCRAFT
| Applicant | Pennsylvania Association For the Blind, Washington PA, US |
| Decision | Substantially Equivalent, Mar 11, 1988 |
| Received | Feb 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880785
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.