510(k) K974733

BOEHRINGER MANNHEIM DIRECT LDL - CHOLESTEROL by Boehringer Mannheim Corp. — Product Code LBR

K974733 is an FDA 510(k) premarket notification submitted by Boehringer Mannheim Corp. for the device "BOEHRINGER MANNHEIM DIRECT LDL - CHOLESTEROL". The FDA issued a decision of Substantially Equivalent on January 26, 1998. The device falls under product code LBR (Ldl & Vldl Precipitation, Hdl), a Class I device regulated under 21 CFR 862.1475. Boehringer Mannheim Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 26, 1998
Date Received
December 18, 1997
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