510(k) K870963 ยท LIO Device, Specimen Collection
MODIFIED PATHFINDER SPECIMEN COLLECTION KIT
| Applicant | Kallestad Diag, A Div. of Erbamont, Inc., Chaska MN, US |
| Decision | Substantially Equivalent, Apr 8, 1987 |
| Received | Mar 10, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870963
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.