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

Chromatography Separation/Zimmerman 17-Ketogenic Steroids

21 CFR 862.1385 / Clinical Chemistry
FDA source (opens on fda.gov)

CDG is the FDA product code for Chromatography Separation/Zimmerman 17-Ketogenic Steroids, a class I device type, regulated under 21 CFR 862.1385. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
CDG
Device name
Chromatography Separation/Zimmerman 17-Ketogenic Steroids
Regulation
21 CFR 862.1385
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 CDG

By decision year
1 clearance under product code CDG with a decision year between 1978 and 1978, 1978 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CDG by decision year
YearClearances
19781

Applicants with the most clearances

Product code CDG
Applicants holding the most 510(k) clearances under product code CDG
ApplicantClearances
Eppendorf-Brinkmann, 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 CDG.