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

ICON STREP B IMMUNOENZYMETRIC ASSAY

K Number: K902991 · Decision Oct 3, 1990
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
43
Applicant Total
63
Review Days
86

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Basic Information

Device Name
ICON STREP B IMMUNOENZYMETRIC ASSAY
K Number
K902991
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3740
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Hybritech, Inc.
Date Received
July 9, 1990
Decision Date
October 3, 1990
Product Code
GTY
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
GTY Antigens, All Groups, Streptococcus Spp.

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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. →