510(k) K973988

RDI HOMOGENEOUS HDL CHOLESTEROL TEST by Reference Diagnostics, Inc. — Product Code LBS

K973988 is an FDA 510(k) premarket notification submitted by Reference Diagnostics, Inc. for the device "RDI HOMOGENEOUS HDL CHOLESTEROL TEST". The FDA issued a decision of Substantially Equivalent on December 22, 1997. 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. Reference Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 22, 1997
Date Received
October 21, 1997
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