510(k) K840677

HDL EZ-TZ3 CHOLESTEROL REAGENT KIT by Preventive Diagnostics Corp. — Product Code LBS

K840677 is an FDA 510(k) premarket notification submitted by Preventive Diagnostics Corp. for the device "HDL EZ-TZ3 CHOLESTEROL REAGENT KIT". The FDA issued a decision of Substantially Equivalent on April 13, 1984. 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. Preventive Diagnostics Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 13, 1984
Date Received
February 15, 1984
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