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

Plate, Cellulose, Tlc

21 CFR 862.2270 / Clinical Chemistry
FDA source (opens on fda.gov)

DKG is the FDA product code for Plate, Cellulose, Tlc, a class I device type, regulated under 21 CFR 862.2270. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
DKG
Device name
Plate, Cellulose, Tlc
Regulation
21 CFR 862.2270
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 DKG

By decision year
1 clearance under product code DKG with a decision year between 1989 and 1989, 1989 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DKG by decision year
YearClearances
19891

Applicants with the most clearances

Product code DKG
Applicants holding the most 510(k) clearances under product code DKG
ApplicantClearances
Syva Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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