FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

IMMUNOCARD TOXINS A & B, MODEL 712050

K Number: K041003 · Decision Aug 20, 2004
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
41
Applicant Total
38
Review Days
123

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
IMMUNOCARD TOXINS A & B, MODEL 712050
K Number
K041003
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2660
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Meridian Bioscience, Inc.
Date Received
April 19, 2004
Decision Date
August 20, 2004
Product Code
LLH
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
LLH Reagents, Clostridium Difficile Toxin

Similar 510(k) Clearances

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

View all

Other Clearances by Meridian Bioscience, Inc.

K Number Device Name
K243922 Revogene
K230901 Premier HpSA Flex (619096)
K222829 Curian® Shiga Toxin
K222779 Revogene
K220480 Revogene
K210976 Curian Campy
K192817 Curian HpSA, Curian Analyzer
DEN180040 Alethia CMV DNA Amplification Assay, Alethia CMV External Control Kit
K182559 PREMIER Platinum HpSA PLUS
K163273 TRU Legionella
Search all 38 clearances from Meridian Bioscience, Inc. →