510(k) K881693 ยท JIS Calibrator, Primary
TERUMO SENSIBEAD EIA PROGESTERONE KIT
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Jun 7, 1988 |
| Received | Apr 19, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881693
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.