510(k) K991664

LDL CHOLESTEROL, PRODUCT NO'S, 124-01, CH102-01 by A.P. Total Care, Inc. — Product Code LBS

K991664 is an FDA 510(k) premarket notification submitted by A.P. Total Care, Inc. for the device "LDL CHOLESTEROL, PRODUCT NO'S, 124-01, CH102-01". The FDA issued a decision of Substantially Equivalent on August 19, 1999. 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. A.P. Total Care, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 19, 1999
Date Received
May 14, 1999
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