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TANDEM-R(R) CARCINOEMBRYONIC ANTIGEN (CEA) ASSAY

FDA premarket approval P840019/S009 · decided 1990-04-17

Approval details

PMA number
P840019
Supplement
S009
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
TANDEM-R(R) CARCINOEMBRYONIC ANTIGEN (CEA) ASSAY
Generic name
SYSTEM, TEST, CARCINOEMBRYONIC ANTIGEN
Applicant
Hybritech, Inc.
Date received
1990-03-14
Decision date
1990-04-17
Days to decision
34 days
Decision code
APPR
Product code
DHX
Advisory committee
Immunology
Expedited review
No
Location
San Diego, CA

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510(k) clearances by this applicant

RecordFirmDate
TANDEM-MP OSTASE IMMUNOENZYMETRIC ASSAY (K972666)Hybritech, Inc.1997-09-11
TANDEM-R OSTASE IMMUNORADIOMETRIC ASSAY (K961573)Hybritech, Inc.1996-08-19
TANDEM-R OSTASE IMMUNORADIOMETRIC ASSAY (K930810)Hybritech, Inc.1994-01-11
TANDEM-E IGE II CALIBRATION VERIFICATION SET (K922754)Hybritech, Inc.1993-02-17
HYBRITECH STRATUS PAP FLUOROMETRIC ENZYME IMMUNO (K921745)Hybritech, Inc.1992-07-30
TANDEM-E FERRITIN CALIBRATION VERIFICATION CONROL (K921252)Hybritech, Inc.1992-07-17
TANDEM-E HCG CALIBRATION VERIFICATION CONTROL SET (K920556)Hybritech, Inc.1992-07-17
TANDEM ICON QSR CKMB IMMUNOENZYMETRIC ASSAY (K921763)Hybritech, Inc.1992-06-09