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

Thin Layer Chromatography, Propoxyphene

21 CFR 862.3700 / Clinical Toxicology
FDA source (opens on fda.gov)

DPN is the FDA product code for Thin Layer Chromatography, Propoxyphene, a class II device type, regulated under 21 CFR 862.3700. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
DPN
Device name
Thin Layer Chromatography, Propoxyphene
Regulation
21 CFR 862.3700
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 DPN

By decision year
1 clearance under product code DPN with a decision year between 2004 and 2004, 2004 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DPN by decision year
YearClearances
20041

Applicants with the most clearances

Product code DPN
Applicants holding the most 510(k) clearances under product code DPN
ApplicantClearances
Arrow Intl., Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code