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

Adsorbents, Ion-Exchange

21 CFR 862.2230 / Clinical Chemistry
FDA source (opens on fda.gov)

DKO is the FDA product code for Adsorbents, Ion-Exchange, a class I device type, regulated under 21 CFR 862.2230. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
DKO
Device name
Adsorbents, Ion-Exchange
Regulation
21 CFR 862.2230
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 DKO

By decision year
1 clearance under product code DKO with a decision year between 1987 and 1987, 1987 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DKO by decision year
YearClearances
19871

Applicants with the most clearances

Product code DKO
Applicants holding the most 510(k) clearances under product code DKO
ApplicantClearances
Molecular Biosystems, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code