510(k) K801834

WAKO HDL CHOLESTEROL TEST by Wako Pure Chemical Industries, Ltd. — Product Code LBS

K801834 is an FDA 510(k) premarket notification submitted by Wako Pure Chemical Industries, Ltd. for the device "WAKO HDL CHOLESTEROL TEST". The FDA issued a decision of Substantially Equivalent on September 16, 1980. 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. Wako Pure Chemical Industries, Ltd. has at least 5 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 16, 1980
Date Received
August 1, 1980
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