The following data is part of a premarket notification filed by Ortho-clinical Diagnostics, Inc. with the FDA for Vitros Immunodiagnostic Products Cortisol Assay.
Device ID | K983990 |
510k Number | K983990 |
Device Name: | VITROS IMMUNODIAGNOSTIC PRODUCTS CORTISOL ASSAY |
Classification | Radioimmunoassay, Cortisol |
Applicant | Ortho-Clinical Diagnostics, Inc. 100 INDIGO CREEK DR. Rochester, NY 14626 -5101 |
Contact | Anne Zavertnik |
Correspondent | Anne Zavertnik Ortho-Clinical Diagnostics, Inc. 100 INDIGO CREEK DR. Rochester, NY 14626 -5101 |
Product Code | CGR |
CFR Regulation Number | 862.1205 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-11-09 |
Decision Date | 1998-12-29 |
Summary: | summary |