510(k) K990036

CARESIDE LYTES, CARESIDE ANALLYZER MODEL 1000 by Careside, Inc. — Product Code JGS

K990036 is an FDA 510(k) premarket notification submitted by Careside, Inc. for the device "CARESIDE LYTES, CARESIDE ANALLYZER MODEL 1000". The FDA issued a decision of Substantially Equivalent on March 18, 1999. The device falls under product code JGS (Electrode, Ion Specific, Sodium), a Class II device regulated under 21 CFR 862.1665. Careside, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 18, 1999
Date Received
January 6, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrode, Ion Specific, Sodium
Device Class
Class II
Regulation Number
862.1665
Review Panel
CH
Submission Type