510(k) K885203

TECHNICON DAX(TM) SYSTEM by Technicon Instruments Corp. — Product Code JJG

K885203 is an FDA 510(k) premarket notification submitted by Technicon Instruments Corp. for the device "TECHNICON DAX(TM) SYSTEM". The FDA issued a decision of Substantially Equivalent on March 28, 1989. The device falls under product code JJG (Analyzer, Chemistry, Centrifugal, For Clinical Use), a Class I device regulated under 21 CFR 862.2140. Technicon Instruments Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 28, 1989
Date Received
December 19, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Analyzer, Chemistry, Centrifugal, For Clinical Use
Device Class
Class I
Regulation Number
862.2140
Review Panel
CH
Submission Type