510(k) K013466

SPIFE 2000/3000 LIPOPROTEIN; MODEL# 3340, 3341, 3342, 3343 by Helena Laboratories — Product Code JHO

K013466 is an FDA 510(k) premarket notification submitted by Helena Laboratories for the device "SPIFE 2000/3000 LIPOPROTEIN; MODEL# 3340, 3341, 3342, 3343". The FDA issued a decision of Substantially Equivalent on December 21, 2001. The device falls under product code JHO (Electrophoretic Separation, Lipoproteins), a Class I device regulated under 21 CFR 862.1475. Helena Laboratories has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 21, 2001
Date Received
October 18, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrophoretic Separation, Lipoproteins
Device Class
Class I
Regulation Number
862.1475
Review Panel
CH
Submission Type