The following data is part of a premarket notification filed by Serono-baker Diagnostics, Inc. with the FDA for Estradiol Serozyme Immunoenzymetric Assay.
| Device ID | K896145 |
| 510k Number | K896145 |
| Device Name: | ESTRADIOL SEROZYME IMMUNOENZYMETRIC ASSAY |
| Classification | Radioimmunoassay, Estradiol |
| Applicant | SERONO-BAKER DIAGNOSTICS, INC. 100 CASCADE DR. Allentown, PA 18103 -9562 |
| Contact | Ronald E Bowman |
| Correspondent | Ronald E Bowman SERONO-BAKER DIAGNOSTICS, INC. 100 CASCADE DR. Allentown, PA 18103 -9562 |
| Product Code | CHP |
| CFR Regulation Number | 862.1260 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-10-23 |
| Decision Date | 1989-12-27 |