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
LAGClass II

High Pressure Liquid Chromatography, Methamphetamine

21 CFR 862.3610 / Clinical Toxicology
FDA source (opens on fda.gov)

LAG is the FDA product code for High Pressure Liquid Chromatography, Methamphetamine, a class II device type, regulated under 21 CFR 862.3610. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LAG
Device name
High Pressure Liquid Chromatography, Methamphetamine
Regulation
21 CFR 862.3610
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 LAG

By decision year
4 clearances under product code LAG with a decision year between 1998 and 2008, 1998 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LAG by decision year
YearClearances
19981
19991
20071
20081

Applicants with the most clearances

Product code LAG
Applicants holding the most 510(k) clearances under product code LAG
ApplicantClearances
Princeton BioMeditech Corp.3
American Bio Medica Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code