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

Liquid Chromatography, Morphine

21 CFR 862.3640 / Clinical Toxicology
FDA source (opens on fda.gov)

DPK is the FDA product code for Liquid Chromatography, Morphine, a class II device type, regulated under 21 CFR 862.3640. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
DPK
Device name
Liquid Chromatography, Morphine
Regulation
21 CFR 862.3640
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
2
Ingested recalls
0

Clearances, product code DPK

By decision year
2 clearances under product code DPK with a decision year between 2000 and 2000, 2000 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code DPK by decision year
YearClearances
20002

Applicants with the most clearances

Product code DPK
Applicants holding the most 510(k) clearances under product code DPK
ApplicantClearances
Alfa Scientific Designs, Inc.2

Companies listing this code with FDA

Companies whose registered establishments list this code