510(k) K041927

LDL/ADVANCE ASSAY, CAT. NO. 279-20, 279-40 by Diagnostic Chemicals , Ltd. — Product Code MRR

K041927 is an FDA 510(k) premarket notification submitted by Diagnostic Chemicals , Ltd. for the device "LDL/ADVANCE ASSAY, CAT. NO. 279-20, 279-40". The FDA issued a decision of Substantially Equivalent on November 23, 2004. The device falls under product code MRR (System, Test, Low Density, Lipoprotein), a Class I device regulated under 21 CFR 862.1475. Diagnostic Chemicals , Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 23, 2004
Date Received
July 19, 2004
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Test, Low Density, Lipoprotein
Device Class
Class I
Regulation Number
862.1475
Review Panel
CH
Submission Type