510(k) K100010

HDL CHOLESTEROL (HDLX) ASSAY by Beckman Coulter, Inc. — Product Code LBS

K100010 is an FDA 510(k) premarket notification submitted by Beckman Coulter, Inc. for the device "HDL CHOLESTEROL (HDLX) ASSAY". The FDA issued a decision of Substantially Equivalent on May 14, 2010. 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. Beckman Coulter, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 14, 2010
Date Received
January 4, 2010
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