510(k) K904075

CLINICAL CHEMISTRY CONTROL by Phoenix Diagnostics, Inc. — Product Code JJY

K904075 is an FDA 510(k) premarket notification submitted by Phoenix Diagnostics, Inc. for the device "CLINICAL CHEMISTRY CONTROL". The FDA issued a decision of Substantially Equivalent on December 6, 1990. The device falls under product code JJY (Multi-Analyte Controls, All Kinds (Assayed)), a Class I device regulated under 21 CFR 862.1660. Phoenix Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 6, 1990
Date Received
September 4, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Multi-Analyte Controls, All Kinds (Assayed)
Device Class
Class I
Regulation Number
862.1660
Review Panel
CH
Submission Type