510(k) K993771

CARESIDE DIRECT BILIRUBIN by Careside, Inc. — Product Code CIG

K993771 is an FDA 510(k) premarket notification submitted by Careside, Inc. for the device "CARESIDE DIRECT BILIRUBIN". The FDA issued a decision of Substantially Equivalent on December 27, 1999. The device falls under product code CIG (Diazo Colorimetry, Bilirubin), a Class II device regulated under 21 CFR 862.1110. Careside, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 27, 1999
Date Received
November 8, 1999
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