510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
LFIClass II

High Pressure Liquid Chromatography, Tricyclic Antidepressant Drugs

21 CFR 862.3910 / Clinical Toxicology
FDA source (opens on fda.gov)

LFI is the FDA product code for High Pressure Liquid Chromatography, Tricyclic Antidepressant Drugs, a class II device type, regulated under 21 CFR 862.3910. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LFI
Device name
High Pressure Liquid Chromatography, Tricyclic Antidepressant Drugs
Regulation
21 CFR 862.3910
Device class
Class II
Review panel
Clinical Toxicology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
4
Ingested recalls
0

Clearances, product code LFI

By decision year
4 clearances under product code LFI with a decision year between 1980 and 1995, 1995 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code LFI by decision year
YearClearances
19801
19941
19952

Applicants with the most clearances

Product code LFI
Applicants holding the most 510(k) clearances under product code LFI
ApplicantClearances
Bio-Rad2
Biosite Incorporated1
Technicon Instruments Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code