510(k) K981899

CARESIDE HDL-CHOLESTEROL by Exigent Diagnostics, Inc. — Product Code LBS

K981899 is an FDA 510(k) premarket notification submitted by Exigent Diagnostics, Inc. for the device "CARESIDE HDL-CHOLESTEROL". The FDA issued a decision of Substantially Equivalent on July 14, 1998. 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. Exigent Diagnostics, Inc. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 14, 1998
Date Received
June 1, 1998
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