510(k) K954778

CHOLESTECH LDX SYSTEM by Cholestech Corp. — Product Code LBS

K954778 is an FDA 510(k) premarket notification submitted by Cholestech Corp. for the device "CHOLESTECH LDX SYSTEM". The FDA issued a decision of Substantially Equivalent on November 24, 1995. 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. Cholestech Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 24, 1995
Date Received
September 19, 1995
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