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
DITClass II

Thin Layer Chromatography, Amphetamine

21 CFR 862.3100 / Clinical Toxicology
FDA source (opens on fda.gov)

DIT is the FDA product code for Thin Layer Chromatography, Amphetamine, a class II device type, regulated under 21 CFR 862.3100. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
DIT
Device name
Thin Layer Chromatography, Amphetamine
Regulation
21 CFR 862.3100
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 DIT

By decision year
4 clearances under product code DIT with a decision year between 1979 and 1997, 1979 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DIT by decision year
YearClearances
19791
19901
19911
19971

Applicants with the most clearances

Product code DIT
Applicants holding the most 510(k) clearances under product code DIT
ApplicantClearances
Siemens Healthcare Diagnostics Inc.1
Drug Screening Systems, Inc.1
Phamatech Inc.1
Technical Resources, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code