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

Tanks, Developing, Tlc

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

DKK is the FDA product code for Tanks, Developing, 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
DKK
Device name
Tanks, Developing, 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
Yes
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code DKK

By decision year
1 clearance under product code DKK with a decision year between 1981 and 1981, 1981 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DKK by decision year
YearClearances
19811

Applicants with the most clearances

Product code DKK
Applicants holding the most 510(k) clearances under product code DKK
ApplicantClearances
Marion Laboratories, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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