The following data is part of a premarket notification filed by Biosite Incorporated with the FDA for Triage Cardiac Calibration Verification Controls, Triage Cardio Profiler Calibration Verficication Controls.
Device ID | K030088 |
510k Number | K030088 |
Device Name: | TRIAGE CARDIAC CALIBRATION VERIFICATION CONTROLS, TRIAGE CARDIO PROFILER CALIBRATION VERFICICATION CONTROLS |
Classification | Multi-analyte Controls, All Kinds (assayed) |
Applicant | BIOSITE INCORPORATED 11030 ROSELLE ST. San Diego, CA 92121 |
Contact | Jeffrey R Dahlen |
Correspondent | Jeffrey R Dahlen BIOSITE INCORPORATED 11030 ROSELLE ST. San Diego, CA 92121 |
Product Code | JJY |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-01-10 |
Decision Date | 2003-01-17 |
Summary: | summary |