510(k) K895381

HDL SINGLES by Trace America, Inc. — Product Code LBR

K895381 is an FDA 510(k) premarket notification submitted by Trace America, Inc. for the device "HDL SINGLES". The FDA issued a decision of Substantially Equivalent on November 8, 1989. The device falls under product code LBR (Ldl & Vldl Precipitation, Hdl), a Class I device regulated under 21 CFR 862.1475. Trace America, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 8, 1989
Date Received
August 29, 1989
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