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

CEFOTAXIME/CLAVULANIC, 30/10UG, BBL SENSI-DISC AND CEFTAZIDIME/CLAVULANIC ACID, 30/10UG, BBL SENSI-DISC

K Number: K993577 · Decision Dec 1, 1999
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
327
Applicant Total
33
Review Days
41

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Basic Information

Device Name
CEFOTAXIME/CLAVULANIC, 30/10UG, BBL SENSI-DISC AND CEFTAZIDIME/CLAVULANIC ACID, 30/10UG, BBL SENSI-DISC
K Number
K993577
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.1620
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Becton Dickinson Microbiology Systems
Date Received
October 21, 1999
Decision Date
December 1, 1999
Product Code
JTN
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
JTN Susceptibility Test Discs, Antimicrobial

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K972098 FOSFOMYCIN, 200 MG, SENSI-DISC
K970385 SPARFLOZACIN, 5 MCG, SENSI-DISC
K970212 LEVOFLOXACIN, 5MCG, SENSI-DISC
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