510(k) K901226

CHEM 1 CLINICAL ANALYZER (METHOD URINE CALCIUM) by Technicon Instruments Corp. — Product Code CIC

K901226 is an FDA 510(k) premarket notification submitted by Technicon Instruments Corp. for the device "CHEM 1 CLINICAL ANALYZER (METHOD URINE CALCIUM)". The FDA issued a decision of Substantially Equivalent on April 19, 1990. The device falls under product code CIC (Cresolphthalein Complexone, Calcium), a Class II device regulated under 21 CFR 862.1145. Technicon Instruments Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 19, 1990
Date Received
March 14, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cresolphthalein Complexone, Calcium
Device Class
Class II
Regulation Number
862.1145
Review Panel
CH
Submission Type