The following data is part of a premarket notification filed by Serono-baker Diagnostics, Inc. with the FDA for Sr1 Estradiol Enzyme Immunoassay.
Device ID | K911396 |
510k Number | K911396 |
Device Name: | SR1 ESTRADIOL ENZYME IMMUNOASSAY |
Classification | Radioimmunoassay, Estradiol |
Applicant | SERONO-BAKER DIAGNOSTICS, INC. 100 CASCADE DR. Allentown, PA 18103 -9562 |
Contact | David B Thomas |
Correspondent | David B Thomas 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 | 1991-03-29 |
Decision Date | 1991-05-28 |