510(k) K983119 ยท LIO Device, Specimen Collection
ENTERO-TEST HP, MODEL #102-01
| Applicant | Hdc Corp., San Jose CA, US |
| Decision | Substantially Equivalent, Mar 15, 1999 |
| Received | Sep 8, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983119
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.