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

BILIRUBIN, TOTAL AND DIRECT, PRODUCT NO, 122-01, 122-02, 122-03, 122-04

K Number: K991866 · Decision Aug 2, 1999
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
234
Applicant Total
18
Review Days
62

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Basic Information

Device Name
BILIRUBIN, TOTAL AND DIRECT, PRODUCT NO, 122-01, 122-02, 122-03, 122-04
K Number
K991866
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1110
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
A.P. Total Care, Inc.
Date Received
June 1, 1999
Decision Date
August 2, 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

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Other Clearances by A.P. Total Care, Inc.

K Number Device Name
K991246 FRUCTOSAMINE, MODEL FR 106-01
K991762 ALKALINE PHOPHATASE (ALP), PRODUCT NO'S 118-01, 118-02
K991761 MAGNESIUM PRODUCT NO'S, 112-01, 112-02
K991664 LDL CHOLESTEROL, PRODUCT NO'S, 124-01, CH102-01
K991665 HDL CHOLESTEROL, PRODUCT NO'S 124-01, CH102-01
K991867 INORGANIC PHOSPHORUS (IP), PRODUCT NO'S, 112-01, 112-02
K991870 ELECTROLYTES (NA+, K+, CL-), PRODUCT NO'S 114-01, 114-02, 114-03
K991663 AST/SGOT
K991666 TIBC, PRODUCT NO'S 123-0, 123-02, FE109-01, FE109-02
K991247 URIC ACID, MODEL UA112-01
Search all 18 clearances from A.P. Total Care, Inc. →