510(k) K953861

HICHEM ISE INTDERNAL REFERENCE KIT 70009 by Hichem Diagnostics — Product Code CGZ

K953861 is an FDA 510(k) premarket notification submitted by Hichem Diagnostics for the device "HICHEM ISE INTDERNAL REFERENCE KIT 70009". The FDA issued a decision of Substantially Equivalent on September 6, 1995. The device falls under product code CGZ (Electrode, Ion-Specific, Chloride), a Class II device regulated under 21 CFR 862.1170. Hichem Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 6, 1995
Date Received
August 17, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrode, Ion-Specific, Chloride
Device Class
Class II
Regulation Number
862.1170
Review Panel
CH
Submission Type