The following data is part of a premarket notification filed by Biosite Incorporated with the FDA for The Triage Ii.
| Device ID | K924476 |
| 510k Number | K924476 |
| Device Name: | THE TRIAGE II |
| Classification | Enzyme Immunoassay, Amphetamine |
| Applicant | BIOSITE INCORPORATED 11030 ROSELLE ST. San Diego, CA 92121 |
| Contact | John F Bruni |
| Correspondent | John F Bruni BIOSITE INCORPORATED 11030 ROSELLE ST. San Diego, CA 92121 |
| Product Code | DKZ |
| CFR Regulation Number | 862.3100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-09-03 |
| Decision Date | 1993-01-22 |