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

RADIAS ANA SCREEN ENZYME IMMUNOASSAY

K Number: K941509 · Decision Jun 30, 1994
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
111
Applicant Total
319
Review Days
93

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
RADIAS ANA SCREEN ENZYME IMMUNOASSAY
K Number
K941509
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bio-Rad
Date Received
March 29, 1994
Decision Date
June 30, 1994
Product Code
LJM
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
LJM Antinuclear Antibody (Enzyme-Labeled), Antigen, Controls

Similar 510(k) Clearances

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

View all

Other Clearances by Bio-Rad

K Number Device Name
K171061 MRSASelect II
K122187 VRESELECT CULTURE MEDIUM
K103684 VRESELECT CULTURE MEDIUM
K093678 PLATELIA ASPERGILLUS EIA MODEL 62793
K100589 MRSA SELECT - SKIN AND SOFT TISSUE WOUND SPECIMENS
K081362 PLATELIA LYME IGM
K081212 MRSASELECT - EXTENDED INCUBATION
K080012 PLATELIA LYME IGG ASSAY
K070361 MRSASELECT
K060641 PLATELIA ASPERGILLUS EIA, MODEL 62793
Search all 319 clearances from Bio-Rad →