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

STANBIO SYPHILIS RPR TEST, NO. 1170

K Number: K880144 · Decision May 23, 1988
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
31
Applicant Total
47
Review Days
131

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Basic Information

Device Name
STANBIO SYPHILIS RPR TEST, NO. 1170
K Number
K880144
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3820
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Stanbio Laboratory
Date Received
January 13, 1988
Decision Date
May 23, 1988
Product Code
GMQ
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
GMQ Antigens, Nontreponemal, All

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Other Clearances by Stanbio Laboratory

K Number Device Name
K090093 STANBIO LABORATORY HEMOPOINT H2 DM HEMOGLOBIN MEASUREMENT SYSTEM
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 →