The following data is part of a premarket notification filed by Serono-baker Diagnostics, Inc. with the FDA for Sri(tm) Cortisol Enzyme Immunoassay(mag Sol Phase).
Device ID | K914886 |
510k Number | K914886 |
Device Name: | SRI(TM) CORTISOL ENZYME IMMUNOASSAY(MAG SOL PHASE) |
Classification | Radioimmunoassay, Cortisol |
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 | CGR |
CFR Regulation Number | 862.1205 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-10-30 |
Decision Date | 1992-03-02 |