FDA 510(k) FDA class 1 Substantially Equivalent 🇪🇸 Spain

RHEUMAGEN ASO T-CONTROL

K Number: K904311 · Decision Jan 25, 1991
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
36
Applicant Total
16
Review Days
128

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Basic Information

Device Name
RHEUMAGEN ASO T-CONTROL
K Number
K904311
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3720
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Biokit USA, Inc.
Date Received
September 19, 1990
Decision Date
January 25, 1991
Product Code
GTQ
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
GTQ Antistreptolysin - Titer/Streptolysin O Reagent

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GTQ), ordered by most recent decision date.

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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
K904312 RHEUMAGEN CRP T-CONTROL
K896433 MODIFIED RUBAGEN
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. →