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

TANDEM-E -FER IMMUNOENZYMETRIC KIT

K Number: K823871 · Decision Feb 25, 1983
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
86
Applicant Total
63
Review Days
64

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Basic Information

Device Name
TANDEM-E -FER IMMUNOENZYMETRIC KIT
K Number
K823871
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5340
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Hybritech, Inc.
Date Received
December 23, 1982
Decision Date
February 25, 1983
Product Code
DBF
Advisory Committee
Immunology
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
DBF Ferritin, Antigen, Antiserum, Control

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Other Clearances by Hybritech, Inc.

K Number Device Name
K972666 TANDEM-MP OSTASE IMMUNOENZYMETRIC ASSAY
K961573 TANDEM-R OSTASE IMMUNORADIOMETRIC ASSAY
K930810 TANDEM-R OSTASE IMMUNORADIOMETRIC ASSAY
K922754 TANDEM-E IGE II CALIBRATION VERIFICATION SET
K921745 HYBRITECH STRATUS PAP FLUOROMETRIC ENZYME IMMUNO
K921252 TANDEM-E FERRITIN CALIBRATION VERIFICATION CONROL
K920556 TANDEM-E HCG CALIBRATION VERIFICATION CONTROL SET
K921763 TANDEM ICON QSR CKMB IMMUNOENZYMETRIC ASSAY
K912439 TANDEM-E TSH CALIBRATION VERIFICATION CONTROL SET
K911417 ICON STREP B IMMUNOENZYMETRIC ASSAY
Search all 63 clearances from Hybritech, Inc. →