510(k) K902675

MULTI ANALYTE MIXTURE, CALIBRATORS by Phoenix Diagnostics, Inc. — Product Code JIX

K902675 is an FDA 510(k) premarket notification submitted by Phoenix Diagnostics, Inc. for the device "MULTI ANALYTE MIXTURE, CALIBRATORS". The FDA issued a decision of Substantially Equivalent on July 31, 1990. The device falls under product code JIX (Calibrator, Multi-Analyte Mixture), a Class II device regulated under 21 CFR 862.1150. Phoenix Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 31, 1990
Date Received
June 19, 1990
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