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

RPR TEST REDITEST

K Number: K843741 · Decision Oct 25, 1984
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
8
Applicant Total
16
Review Days
30

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Basic Information

Device Name
RPR TEST REDITEST
K Number
K843741
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3820
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Biokit USA, Inc.
Date Received
September 25, 1984
Decision Date
October 25, 1984
Product Code
GMP
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
GMP Antisera, Control For Nontreponemal Tests

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K910686 RHEUMAJET CRP
K904311 RHEUMAGEN ASO T-CONTROL
K904312 RHEUMAGEN CRP T-CONTROL
K896433 MODIFIED RUBAGEN
K896271 QUANTEX RF PLUS (LATEX, BUFFER STANDARD, CONTROL)
K896272 QUANTEX CRP PLUS (LATEX, BUFFER, STANDARD, CONTROL
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