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

RHEUMAJET RF

K Number: K910539 · Decision Apr 5, 1991
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
143
Applicant Total
16
Review Days
67

Basic Information

Device Name
RHEUMAJET RF
K Number
K910539
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5775
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
BIOKIT USA, INC.
Date Received
January 28, 1991
Decision Date
April 5, 1991
Product Code
DHR
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DHR System, Test, Rheumatoid Factor

Similar 510(k) Clearances

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

View all

Other Clearances by BIOKIT USA, INC.

K Number Device Name
K913467 TOXOGEN
K910541 BIOKIT RPR
K904310 RHEUMAGEN RF T-CONTROL
K910686 RHEUMAJET CRP
K904311 RHEUMAGEN ASO T-CONTROL
K904312 RHEUMAGEN CRP T-CONTROL
K896433 MODIFIED RUBAGEN
K896272 QUANTEX CRP PLUS (LATEX, BUFFER, STANDARD, CONTROL
K896271 QUANTEX RF PLUS (LATEX, BUFFER STANDARD, CONTROL)
K894486 QUANTEX ASO PLUS (LATEX,BUFFER STANDARD,CONTROL)
Search all 16 clearances from BIOKIT USA, INC. →