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

DADE RPR CARD TEST

K Number: K811152 · Decision May 15, 1981
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
31
Applicant Total
149
Review Days
18

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Basic Information

Device Name
DADE RPR CARD TEST
K Number
K811152
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3820
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
American Dade
Date Received
April 27, 1981
Decision Date
May 15, 1981
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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K873052 STRATUS(R) HLH FLUOROMETRIC ENZYME IMMUNOASSAY
K872789 PARAMAX URINE/CSF CALIBRATOR
K872195 DATA-FI DIMERTEST LATEX ASSAY
K872196 AQUEOUS BLOOD GAS/ELECTROLYTE CONTR LEV I,II & III
K871972 STRATUS IGE FLUOROMETRIC ENZYME IMMUNOASSAY
K871977 DADE MONI-TROL CHEMISTRY CONTROL/CALIBRATOR
K872050 PARAMAX CHOLESTEROL REAGENT
K872360 DATA-FI FIBRIN(OGEN) DEGRADATION PROD.(FDP)DET SET
Search all 149 clearances from American Dade →