510(k) K021671

JAS HDL CHOLESTEROL (AUTOMATED) REAGENT by Jas Diagnostics, Inc. — Product Code LBS

K021671 is an FDA 510(k) premarket notification submitted by Jas Diagnostics, Inc. for the device "JAS HDL CHOLESTEROL (AUTOMATED) REAGENT". The FDA issued a decision of Substantially Equivalent on July 19, 2002. 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. Jas Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 19, 2002
Date Received
May 21, 2002
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