JRA — Microtitrator, For Clinical Use Class I

FDA Device Classification

FDA product code JRA covers "Microtitrator, For Clinical Use", a Class I medical device regulated under 21 CFR 862.2680. 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
JRA
Device Class
Class I
Regulation Number
862.2680
Submission Type
Review Panel
CH
Medical Specialty
Clinical Chemistry
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K963268tecan u.sGENESIS RMPMarch 18, 1997