510(k) K922612

CHOLESTECH LIPID MONITORING SYSTEM, TOTAL CHOLESTE by Cholestech Corp. — Product Code CHH

K922612 is an FDA 510(k) premarket notification submitted by Cholestech Corp. for the device "CHOLESTECH LIPID MONITORING SYSTEM, TOTAL CHOLESTE". The FDA issued a decision of Substantially Equivalent on June 24, 1992. The device falls under product code CHH (Enzymatic Esterase--Oxidase, Cholesterol), a Class I device regulated under 21 CFR 862.1175. Cholestech Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 24, 1992
Date Received
June 2, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzymatic Esterase--Oxidase, Cholesterol
Device Class
Class I
Regulation Number
862.1175
Review Panel
CH
Submission Type