Home › Device types › LFH
U.V. Spectrometry, Tricyclic Antidepressant Drugs
FDA product code LFH · Class 2 · Clinical Toxicology
29
Registered devices
1
Adverse events
3
Recalls
6
510(k) clearances
Devices with this code
QuikScreen — SYNTRON BIORESEARCH, INC.ACCUTEST Drug Test Cup 13-Panel CLIA-Waived — JANT PHARMACAL CORPORATIONQTEST 12 (25 Pack) — MEDIMPEX UNITED, INCAlere iCup Dx 14 — Instant Technologies, Inc.Status Toxi Cup — Lifesign L.L.C.Fastect II Drug Screen Dipstick Test — BRANAN MEDICAL CORPORATIONTD TRICYC ANTIDEPRESSANT ASSAY, TCA — Siemens Healthcare Diagnostics Inc.ADVIA® Chemistry TCA — Siemens Healthcare Diagnostics Inc.LifeSign QuikScreen 11 — Lifesign L.L.C.ACCUTEST Drug Test Cup 12-Panel CLIA-Waived — JANT PHARMACAL CORPORATIONACCUTEST - 5 Drug Test Cup *CLIA-Waived* — JANT PHARMACAL CORPORATIONQuikScreen — SYNTRON BIORESEARCH, INC.QuikScreen Multi 12 Drug Cup Test — SYNTRON BIORESEARCH, INC.DRI Tricyclics Serum Tox Assay — Microgenics CorporationQuikScreen — SYNTRON BIORESEARCH, INC.QuikScreen — SYNTRON BIORESEARCH, INC.QTEST 11 (25 pack) — MEDIMPEX UNITED, INCStatus Toxi Cup 13+4 — Lifesign L.L.C.Fastect II Drug Screen Dipstick Test — AMEDITECH INC.QuikScreen — SYNTRON BIORESEARCH, INC.Alere iScreen Dx — Instant Technologies, Inc.QuikScreen Multi 11 Drug Cup Test — SYNTRON BIORESEARCH, INC.ACCUTEST - 6 Drug Cup — JANT PHARMACAL CORPORATIONAlere iScreen Dx — Instant Technologies, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-12-15 | Ameditech Inc | The kit box label incorrectly identifies Phencyclidine (PCP), where it should list Tricyclic Antidepressants (TCA) as one of the 10 drug analytes included in th |
| 2017-06-26 | Ameditech Inc | The kit box label incorrectly identifies PCP (instead of TCA) as one of the 10 drug analytes included in the kit. The pouch label, product insert, and the devic |
| 2003-11-17 | Abbott Health Products, Inc. | Drug product cross reacts with the Tricyclic Antidepressants (TCA) assay. |
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