510(k) K070104

PROLYTE ELECTROLYTE ANALYZER by Diamond Diagnostics, Inc. — Product Code JGS

K070104 is an FDA 510(k) premarket notification submitted by Diamond Diagnostics, Inc. for the device "PROLYTE ELECTROLYTE ANALYZER". The FDA issued a decision of Substantially Equivalent on May 7, 2008. The device falls under product code JGS (Electrode, Ion Specific, Sodium), a Class II device regulated under 21 CFR 862.1665. Diamond Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 7, 2008
Date Received
January 10, 2007
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