510(k) K934039

INTERSECT SYSTEMS HDL CHOLESTEROL REAGENT SET by Intersect Systems, Inc. — Product Code LBR

K934039 is an FDA 510(k) premarket notification submitted by Intersect Systems, Inc. for the device "INTERSECT SYSTEMS HDL CHOLESTEROL REAGENT SET". The FDA issued a decision of Substantially Equivalent on November 16, 1993. The device falls under product code LBR (Ldl & Vldl Precipitation, Hdl), a Class I device regulated under 21 CFR 862.1475. Intersect Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 16, 1993
Date Received
August 18, 1993
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