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
DPMClass I

Columns, Liquid Chromatography

21 CFR 862.2260 / Clinical Chemistry
FDA source (opens on fda.gov)

DPM is the FDA product code for Columns, Liquid Chromatography, a class I device type, regulated under 21 CFR 862.2260. As of , FDA records hold 16 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
DPM
Device name
Columns, Liquid Chromatography
Regulation
21 CFR 862.2260
Device class
Class I
Review panel
Clinical Chemistry
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
16
Ingested recalls
0

Clearances, product code DPM

By decision year
16 clearances under product code DPM with a decision year between 1976 and 1995, 1988 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code DPM by decision year
YearClearances
19761
19801
19811
19821
19831
19841
19862
19871
19883
19893
19951

Applicants with the most clearances

Product code DPM
Applicants holding the most 510(k) clearances under product code DPM
ApplicantClearances
Supelco, Inc.10
Waters Chemical Products2
Brinkman Instruments, Inc.1
Chimera Research & Chemical, Inc.1
Hamilton Co1
EMD Millipore Corporation1

Companies listing this code with FDA

Companies whose registered establishments list this code