510(k) K940571

SYNERMEDIR CAL I AND SYNERMED IR CAL II by Synermed, Inc. — Product Code JIX

K940571 is an FDA 510(k) premarket notification submitted by Synermed, Inc. for the device "SYNERMEDIR CAL I AND SYNERMED IR CAL II". The FDA issued a decision of Substantially Equivalent on April 21, 1994. The device falls under product code JIX (Calibrator, Multi-Analyte Mixture), a Class II device regulated under 21 CFR 862.1150. Synermed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 21, 1994
Date Received
February 8, 1994
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