CDG — Chromatography Separation/Zimmerman 17-Ketogenic Steroids Class I

FDA Device Classification

FDA product code CDG covers "Chromatography Separation/Zimmerman 17-Ketogenic Steroids", a Class I medical device regulated under 21 CFR 862.1385. Submissions are reviewed by the Clinical Chemistry panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
CDG
Device Class
Class I
Regulation Number
862.1385
Submission Type
Review Panel
CH
Medical Specialty
Clinical Chemistry
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K772337eppendorf-brinkmannURINARY 17-KETOSTERIOD/17January 12, 1978