510(k) K932766

HDL-CHOLESTRAL(DEXTRAN SULFATE/MAGNESIUM) by Diagnostic Chemicals, Ltd. (Usa) — Product Code LBR

K932766 is an FDA 510(k) premarket notification submitted by Diagnostic Chemicals, Ltd. (Usa) for the device "HDL-CHOLESTRAL(DEXTRAN SULFATE/MAGNESIUM)". The FDA issued a decision of Substantially Equivalent on December 10, 1993. The device falls under product code LBR (Ldl & Vldl Precipitation, Hdl), a Class I device regulated under 21 CFR 862.1475. Diagnostic Chemicals, Ltd. (Usa) has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 10, 1993
Date Received
June 8, 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