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VITEK 2 GRAM NEGATIVE AST FOR CEFEPIME

FDA premarket approval N50510/S130 · decided 2000-05-18

Approval details

PMA number
N50510
Supplement
S130
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
VITEK 2 GRAM NEGATIVE AST FOR CEFEPIME
Generic name
Susceptibility test cards, antimicrobial
Applicant
Biomerieux Vitek, Inc.
Date received
2000-04-03
Decision date
2000-05-18
Days to decision
45 days
Decision code
APPR
Product code
LTW
Advisory committee
Microbiology
Expedited review
No
Location
Hazelwood, MO
Statement
APPROVAL FOR THE ADDITION OF THE ANTIBIOTIC CEFEPIME AT CONCENTRATIONS OF 2, 8, 16 AND 32 MICROGRAMS/ML TO THE VITEK 2 GRAM NEGATIVE SUSCEPTIBILITY TEST CARDS FOR USE IN THE VITEK 2 SYSTEM.

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510(k) clearances by this applicant

RecordFirmDate
VIDAS D-DIMER (DD) ASSAY (K973819)Biomerieux Vitek, Inc.1998-03-10
VIDAS ROTAVIRUS (RTV) ASSAY (K972895)Biomerieux Vitek, Inc.1997-10-03
VIDAS ROTAVIRUS ASSAY (K965092)Biomerieux Vitek, Inc.1997-05-05
VIDAS C. DIFFICILE TOXIN A II ASSAY (K964887)Biomerieux Vitek, Inc.1997-04-08
VIDAS CHLAMYDIA BLOCKING ASSAY (K955627)Biomerieux Vitek, Inc.1996-10-07
VIDAS CREATINE KINASE MB ASSAY 30-421 (K962549)Biomerieux Vitek, Inc.1996-08-30
GRAM NEGATIVE IDENTIFICATION PLUS CARD (K962609)Biomerieux Vitek, Inc.1996-08-30
VITEK GRAM POSITIVE IDENTIFICATION CARD (GPI) (K952095)Biomerieux Vitek, Inc.1996-03-12