510(k) K955154

CAL 1 & CAL 2 SOLUTION, FLUSH SOLUTION KIT by Alko Diagnostic Corp. — Product Code JIX

K955154 is an FDA 510(k) premarket notification submitted by Alko Diagnostic Corp. for the device "CAL 1 & CAL 2 SOLUTION, FLUSH SOLUTION KIT". The FDA issued a decision of Substantially Equivalent on December 11, 1995. The device falls under product code JIX (Calibrator, Multi-Analyte Mixture), a Class II device regulated under 21 CFR 862.1150. Alko Diagnostic Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 11, 1995
Date Received
November 13, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Calibrator, Multi-Analyte Mixture
Device Class
Class II
Regulation Number
862.1150
Review Panel
CH
Submission Type