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

TANDEM-E IGE II CALIBRATION VERIFICATION SET

K Number: K922754 · Decision Feb 17, 1993
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
63
Review Days
254

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Basic Information

Device Name
TANDEM-E IGE II CALIBRATION VERIFICATION SET
K Number
K922754
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hybritech, Inc.
Date Received
June 8, 1992
Decision Date
February 17, 1993
Product Code
JJX
Advisory Committee
Clinical Chemistry
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

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K Number Device Name
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K930810 TANDEM-R OSTASE IMMUNORADIOMETRIC ASSAY
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
K902991 ICON STREP B IMMUNOENZYMETRIC ASSAY
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