FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

TANDEM-E FSH IMMUNOENZYMETRIC ASSAY KIT

K Number: K894761 · Decision Sep 13, 1989
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
87
Applicant Total
63
Review Days
48

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Basic Information

Device Name
TANDEM-E FSH IMMUNOENZYMETRIC ASSAY KIT
K Number
K894761
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Hybritech, Inc.
Date Received
July 27, 1989
Decision Date
September 13, 1989
Product Code
CGJ
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
CGJ Radioimmunoassay, Follicle-Stimulating Hormone

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Other Clearances by Hybritech, Inc.

K Number Device Name
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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. →