FDA 510(k) FDA class 2 Substantially Equivalent 🇪🇸 Spain

MODIFIED RUBAGEN

K Number: K896433 · Decision Nov 29, 1989
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
12
Applicant Total
16
Review Days
20

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Basic Information

Device Name
MODIFIED RUBAGEN
K Number
K896433
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3510
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Biokit USA, Inc.
Date Received
November 9, 1989
Decision Date
November 29, 1989
Product Code
LQN
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
LQN Latex Agglutination Assay, Rubella

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Other Clearances by Biokit USA, Inc.

K Number Device Name
K913467 TOXOGEN
K910541 BIOKIT RPR
K904310 RHEUMAGEN RF T-CONTROL
K910539 RHEUMAJET RF
K910686 RHEUMAJET CRP
K904311 RHEUMAGEN ASO T-CONTROL
K904312 RHEUMAGEN CRP T-CONTROL
K896271 QUANTEX RF PLUS (LATEX, BUFFER STANDARD, CONTROL)
K896272 QUANTEX CRP PLUS (LATEX, BUFFER, STANDARD, CONTROL
K894486 QUANTEX ASO PLUS (LATEX,BUFFER STANDARD,CONTROL)
Search all 16 clearances from Biokit USA, Inc. →