510(k) K833160

HDL EZ-TAB by Preventive Diagnostics Corp. — Product Code LBR

K833160 is an FDA 510(k) premarket notification submitted by Preventive Diagnostics Corp. for the device "HDL EZ-TAB". The FDA issued a decision of Substantially Equivalent on February 9, 1984. The device falls under product code LBR (Ldl & Vldl Precipitation, Hdl), a Class I device regulated under 21 CFR 862.1475. Preventive Diagnostics Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 9, 1984
Date Received
September 16, 1983
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