510(k) K850054 ยท CIB Radioimmunoassay, Angiotensin I And Renin
RIANEN ANGIOTENSIN I RADIOIMMUNOASSAY KI
| Applicant | E.I. Dupont DE Nemours & Co., Inc., N. Billerica MA, US |
| Decision | Substantially Equivalent, Mar 29, 1985 |
| Received | Jan 8, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850054
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 12, 2003 | Perkinelmer Life Sciences, Inc. Angiotensin I [125I] Radioimmunoassay Kit, 250 Tube
Catalog Number: NEA104
For in-vitro diagnostic use Terminated |
CIB | None listed |
| Sep 12, 2003 | Perkinelmer Life Sciences, Inc. Angiotensin I [125I] Radioimmunoassay Kit, 500 Tube
Catalog Number: NEA105
For in-vitro diagnostic use Terminated |
CIB | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.