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

Thin Layer Chromatography, Ethosuximide

21 CFR 862.3380 / Clinical Toxicology
FDA source (opens on fda.gov)

DNP is the FDA product code for Thin Layer Chromatography, Ethosuximide, a class II device type, regulated under 21 CFR 862.3380. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
DNP
Device name
Thin Layer Chromatography, Ethosuximide
Regulation
21 CFR 862.3380
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
1
Ingested recalls
0

Clearances, product code DNP

By decision year
1 clearance under product code DNP with a decision year between 1990 and 1990, 1990 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DNP by decision year
YearClearances
19901

Applicants with the most clearances

Product code DNP
Applicants holding the most 510(k) clearances under product code DNP
ApplicantClearances
Pioneering Technologies, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code