510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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LFHClass II

U.V. Spectrometry, Tricyclic Antidepressant Drugs

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

LFH is the FDA product code for U.V. Spectrometry, Tricyclic Antidepressant Drugs, a class II device type, regulated under 21 CFR 862.3910. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and 3 recalls.

Classification record

Product code
LFH
Device name
U.V. Spectrometry, 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
6
Ingested recalls
3

Clearances, product code LFH

By decision year
6 clearances under product code LFH with a decision year between 1995 and 2023, 1998 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code LFH by decision year
YearClearances
19951
19961
19982
20221
20231

Applicants with the most clearances

Product code LFH
Applicants holding the most 510(k) clearances under product code LFH
ApplicantClearances
Diagnostic Reagents, Inc.2
Microgenics Corporation2
Abbott Medical1
Princeton BioMeditech Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code