The following data is part of a premarket notification filed by Diagnostic Reagents, Inc. with the FDA for Tricyclics Serum Tox Assay.
| Device ID | K961393 |
| 510k Number | K961393 |
| Device Name: | TRICYCLICS SERUM TOX ASSAY |
| Classification | U.v. Spectrometry, Tricyclic Antidepressant Drugs |
| Applicant | DIAGNOSTIC REAGENTS, INC. 601 CALIFORNIA AVE. Sunnyvale, CA 94086 |
| Contact | Yuh-geng Tsay, Ph.d. |
| Correspondent | Yuh-geng Tsay, Ph.d. DIAGNOSTIC REAGENTS, INC. 601 CALIFORNIA AVE. Sunnyvale, CA 94086 |
| Product Code | LFH |
| CFR Regulation Number | 862.3910 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-04-11 |
| Decision Date | 1996-06-12 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00630414595849 | K961393 | 000 |
| 00630414551036 | K961393 | 000 |