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

I.M.N. LATEX

K Number: K874678 · Decision Dec 14, 1987
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
58
Applicant Total
16
Review Days
31

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
I.M.N. LATEX
K Number
K874678
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5640
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Biokit USA, Inc.
Date Received
November 13, 1987
Decision Date
December 14, 1987
Product Code
KTN
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
KTN System, Test, Infectious Mononucleosis

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KTN), 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
K910539 RHEUMAJET RF
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
Search all 16 clearances from Biokit USA, Inc. →