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

STANBIO QUICK-TELL MONOCLONAL INDIRECT

K Number: K842544 · Decision Sep 21, 1984
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
95
Applicant Total
47
Review Days
81

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Basic Information

Device Name
STANBIO QUICK-TELL MONOCLONAL INDIRECT
K Number
K842544
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Stanbio Laboratory
Date Received
July 2, 1984
Decision Date
September 21, 1984
Product Code
JHJ
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
JHJ Agglutination Method, Human Chorionic Gonadotropin

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Other Clearances by Stanbio Laboratory

K Number Device Name
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K081719 STANBIO LABORATORY HEMOPOINT H2 HEMOGLOBIN MEASUREMENT SYSTEM
K050266 DIRECT BILIRUBIN LIQUICOLOR AND TOTAL BILIRUBIN LIQUICOLOR
K050283 CREATININE LIQUICOLOR
K042169 STANBIO LABORATORY SIRRUS CLINICAL CHEMISTRY ANALYZER
K041155 WIDE RANGE C-REACTIVE PROTEIN (WR CRP) ASSAY
K032936 DIRECT LDL CHOLESTEROL LIQUID COLOR AND STANBIO DIRECT HDL/LDL CHOLESTEROL CALIBRATOR
K032932 DIRECT HDL-CHOLESTEROL LIQUID COLOR; DIRECT HDL/LDL-CHOLESTEROL CALIBRATOR
K032482 STANBIO LABORATORY HEMOPOINT H2 HEMOGLOBIN MEASUREMENT SYSTEM
K020378 QUPID PLUS E.R.
Search all 47 clearances from Stanbio Laboratory →