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
DMZClass I

Liquid Chromatography, Adsorbent

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

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

Classification record

Product code
DMZ
Device name
Liquid Chromatography, Adsorbent
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
1
Ingested recalls
0

Clearances, product code DMZ

By decision year
1 clearance under product code DMZ with a decision year between 1983 and 1983, 1983 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DMZ by decision year
YearClearances
19831

Applicants with the most clearances

Product code DMZ
Applicants holding the most 510(k) clearances under product code DMZ
ApplicantClearances
Hamilton Co1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code DMZ.