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

HYBRITECH IMMUNOCHEMISTRY ANALYZER

K Number: K852385 · Decision Jul 12, 1985
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
56
Applicant Total
63
Review Days
37

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Basic Information

Device Name
HYBRITECH IMMUNOCHEMISTRY ANALYZER
K Number
K852385
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2170
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Hybritech, Inc.
Date Received
June 5, 1985
Decision Date
July 12, 1985
Product Code
JJF
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
JJF Analyzer, Chemistry, Micro, For Clinical Use

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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. →