510(k) K872050

PARAMAX CHOLESTEROL REAGENT by American Dade — Product Code LBS

K872050 is an FDA 510(k) premarket notification submitted by American Dade for the device "PARAMAX CHOLESTEROL REAGENT". The FDA issued a decision of Substantially Equivalent on July 7, 1987. The device falls under product code LBS (Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl), a Class I device regulated under 21 CFR 862.1475. American Dade has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 7, 1987
Date Received
May 28, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl
Device Class
Class I
Regulation Number
862.1475
Review Panel
CH
Submission Type