510(k) K952179

SYNERMED ISE REAGENTS by Synermed, Inc. — Product Code JGS

K952179 is an FDA 510(k) premarket notification submitted by Synermed, Inc. for the device "SYNERMED ISE REAGENTS". The FDA issued a decision of Substantially Equivalent on June 20, 1995. The device falls under product code JGS (Electrode, Ion Specific, Sodium), a Class II device regulated under 21 CFR 862.1665. Synermed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 20, 1995
Date Received
May 9, 1995
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