510(k) K963939

SYNERMED DIRECT BILIRUBIN REAGENT KIT by Synermed, Inc. — Product Code CIG

K963939 is an FDA 510(k) premarket notification submitted by Synermed, Inc. for the device "SYNERMED DIRECT BILIRUBIN REAGENT KIT". The FDA issued a decision of Substantially Equivalent on December 18, 1996. The device falls under product code CIG (Diazo Colorimetry, Bilirubin), a Class II device regulated under 21 CFR 862.1110. Synermed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 18, 1996
Date Received
October 1, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Diazo Colorimetry, Bilirubin
Device Class
Class II
Regulation Number
862.1110
Review Panel
CH
Submission Type