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

PREMIER-C. DIFFICILE TOXIN A

K Number: K903456 · Decision Oct 1, 1990
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
41
Applicant Total
92
Review Days
61

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
PREMIER-C. DIFFICILE TOXIN A
K Number
K903456
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2660
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Meridian Diagnostics, Inc.
Date Received
August 1, 1990
Decision Date
October 1, 1990
Product Code
LLH
Advisory Committee
Microbiology
Review Advisory Committee
TX
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 Diagnostics, Inc.

K Number Device Name
K993914 PREMIER TOXINS A&B, MODEL 616096
K990263 IMMUNOCARD STAT! E. COLI O157:H7
K984346 PREMIER TYPE SPECIFIC HSV-2 IGG ELISA TEST
K984343 PREMIER TYPE SPECIFIC HSV-1 IGG ELISA TEST
K983255 MODIFICATION TO: PREMIER PLATINUM HPSA
K982764 PREMIER CRYPTOSPORIDIUM
K982711 PREMIER GIARDIA
K980076 PREMIER PLATINUM HPSA
K980077 PARA-PAK SPINCON
K971585 IMMUNOCARD STAT! ROTAVIRUS
Search all 92 clearances from Meridian Diagnostics, Inc. →