JJL — Plasma Viscometer For Clinical Use Class I

FDA Device Classification

FDA product code JJL covers "Plasma Viscometer For Clinical Use", a Class I medical device regulated under 21 CFR 862.2920. 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
JJL
Device Class
Class I
Regulation Number
862.2920
Submission Type
Review Panel
CH
Medical Specialty
Clinical Chemistry
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K883503coulter electronicsCOULTER VISCOMETER IISeptember 19, 1988