FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CARESIDE DIRECT BILIRUBIN

K Number: K993771 · Decision Dec 27, 1999
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
234
Applicant Total
22
Review Days
49

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Basic Information

Device Name
CARESIDE DIRECT BILIRUBIN
K Number
K993771
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1110
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Careside, Inc.
Date Received
November 8, 1999
Decision Date
December 27, 1999
Product Code
CIG
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CIG Diazo Colorimetry, Bilirubin

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CIG), ordered by most recent decision date.

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Other Clearances by Careside, Inc.

K Number Device Name
K020484 CARESIDE LDH
K020486 CARESIDE GGT
K020487 CARESIDE ALT
K020488 CARESIDE TRGLYCERIDE
K002792 CARESIDE CHOLINESTERASE
K001462 CARESIDE HEMOGLOBIN
K993634 CARESIDE ANALYZER
K992475 CARESIDE CO2, TOTAL
K991717 CARESIDE MG
K991371 CARESIDE AMMONIA
Search all 22 clearances from Careside, Inc. →