510(k) K915675

ELECTRODE, ION SPECIFIC by Alko Diagnostic Corp. — Product Code JFP

K915675 is an FDA 510(k) premarket notification submitted by Alko Diagnostic Corp. for the device "ELECTRODE, ION SPECIFIC". The FDA issued a decision of Substantially Equivalent on April 29, 1992. The device falls under product code JFP (Electrode, Ion Specific, Calcium), a Class II device regulated under 21 CFR 862.1145. Alko Diagnostic Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 29, 1992
Date Received
December 19, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrode, Ion Specific, Calcium
Device Class
Class II
Regulation Number
862.1145
Review Panel
CH
Submission Type