The following data is part of a premarket notification filed by Ortho-clinical Diagnostics, Inc. with the FDA for Vitros Immunodiagnostic Products Troponin I Range Verifiers.
Device ID | K992349 |
510k Number | K992349 |
Device Name: | VITROS IMMUNODIAGNOSTIC PRODUCTS TROPONIN I RANGE VERIFIERS |
Classification | Multi-analyte Controls, All Kinds (assayed) |
Applicant | Ortho-Clinical Diagnostics, Inc. 100 INDIGO CREEK DR. Rochester, NY 14626 -5101 |
Contact | Marlene A Shulman |
Correspondent | Marlene A Shulman Ortho-Clinical Diagnostics, Inc. 100 INDIGO CREEK DR. Rochester, NY 14626 -5101 |
Product Code | JJY |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-07-14 |
Decision Date | 1999-08-24 |
Summary: | summary |