510(k) K890984 ยท KIO Slide Stainer, Immersion Type
LINISTAIN SLS
| Applicant | Shandon, Inc., Pittsburgh PA, US |
| Decision | Substantially Equivalent, Apr 4, 1989 |
| Received | Feb 27, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890984
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.