The following data is part of a premarket notification filed by Biosite Incorporated with the FDA for Trigage Profiler S.o.b. Panel, Model 97300.
Device ID | K042723 |
510k Number | K042723 |
Device Name: | TRIGAGE PROFILER S.O.B. PANEL, MODEL 97300 |
Classification | Fibrinogen And Fibrin Split Products, Antigen, Antiserum, Control |
Applicant | BIOSITE INCORPORATED 11030 ROSELLE ST. San Diego, CA 92121 |
Contact | Jerrrey R Dahlen |
Correspondent | Jerrrey R Dahlen BIOSITE INCORPORATED 11030 ROSELLE ST. San Diego, CA 92121 |
Product Code | DAP |
Subsequent Product Code | DDR |
Subsequent Product Code | JHX |
Subsequent Product Code | MMI |
Subsequent Product Code | NBC |
CFR Regulation Number | 864.7320 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-10-01 |
Decision Date | 2004-12-07 |
Summary: | summary |