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

AMS GRAM-NEGATIVE IDENT. CARD

K Number: K834269 · Decision Mar 9, 1984
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
243
Applicant Total
39
Review Days
92

Basic Information

Device Name
AMS GRAM-NEGATIVE IDENT. CARD
K Number
K834269
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2660
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
VITEK SYSTEMS, INC.
Date Received
December 8, 1983
Decision Date
March 9, 1984
Product Code
JTO
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
JTO Discs, Strips And Reagents, Microorganism Differentiation

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K Number Device Name
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K921176 VITEK IMMUNODIAGNOSTIC ASSAY SYSTEM
K920952 VITEK IMMUNODIAG ASSAY SYST(VIDAS) FERRITINE ASSAY
K915884 VIDAS CHLAMYDIA ASSAY, MODIFICATION
K905211 VIDAS CLOSTRIDIUM DIFFICILE TOXIN A (CDA) ASSAY
K912371 BIOMERIEUX RSV DIRECT IF KIT
K910230 LYME-SPOT IF KIT
K910210 SLIDEX MENINGITE-KIT 5
K910304 RAPID CORYNE SYST/IDENTIF OF CORYNEFORM BACTERIA
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