510(k) K914511

TECHNICON AXON(TM) SYSTEM METHODS ANYALYE HDL CHOL by Technicon Instruments Corp. — Product Code LBS

K914511 is an FDA 510(k) premarket notification submitted by Technicon Instruments Corp. for the device "TECHNICON AXON(TM) SYSTEM METHODS ANYALYE HDL CHOL". The FDA issued a decision of Substantially Equivalent on November 27, 1991. The device falls under product code LBS (Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl), a Class I device regulated under 21 CFR 862.1475. Technicon Instruments Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 27, 1991
Date Received
October 9, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl
Device Class
Class I
Regulation Number
862.1475
Review Panel
CH
Submission Type