510(k) K011972

DIRECT BILIRUBIN REAGENT by Intersect Systems, Inc. — Product Code CIG

K011972 is an FDA 510(k) premarket notification submitted by Intersect Systems, Inc. for the device "DIRECT BILIRUBIN REAGENT". The FDA issued a decision of Substantially Equivalent on August 27, 2001. The device falls under product code CIG (Diazo Colorimetry, Bilirubin), a Class II device regulated under 21 CFR 862.1110. Intersect Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 27, 2001
Date Received
June 25, 2001
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