510(k) K020487

CARESIDE ALT by Careside, Inc. — Product Code CKA

K020487 is an FDA 510(k) premarket notification submitted by Careside, Inc. for the device "CARESIDE ALT". The FDA issued a decision of Substantially Equivalent on June 4, 2002. The device falls under product code CKA (Nadh Oxidation/Nad Reduction, Alt/Sgpt), a Class I device regulated under 21 CFR 862.1030. Careside, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 4, 2002
Date Received
February 13, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Nadh Oxidation/Nad Reduction, Alt/Sgpt
Device Class
Class I
Regulation Number
862.1030
Review Panel
CH
Submission Type