510(k) K912823

HIGH DENSITY LIPOPROTEIN CHOLESTEROL by Creative Laboratory Products, Inc. — Product Code LBR

K912823 is an FDA 510(k) premarket notification submitted by Creative Laboratory Products, Inc. for the device "HIGH DENSITY LIPOPROTEIN CHOLESTEROL". The FDA issued a decision of Substantially Equivalent on August 16, 1991. The device falls under product code LBR (Ldl & Vldl Precipitation, Hdl), a Class I device regulated under 21 CFR 862.1475. Creative Laboratory Products, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 16, 1991
Date Received
June 26, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ldl & Vldl Precipitation, Hdl
Device Class
Class I
Regulation Number
862.1475
Review Panel
CH
Submission Type