510(k) K931770 ยท LIO Device, Specimen Collection
PARA-PAK PLUS
| Applicant | Meridian Diagnostics, Inc., Cincinnati OH, US |
| Decision | Substantially Equivalent, Jun 15, 1993 |
| Received | Apr 9, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931770
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.