FDA 510(k) FDA class 2 Substantially Equivalent 🇸🇪 Sweden

ETEST LINEZOLID

K Number: K002139 · Decision Nov 8, 2000
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
1
Applicant Total
64
Review Days
114

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Basic Information

Device Name
ETEST LINEZOLID
K Number
K002139
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.1620
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ab Biodisk
Date Received
July 17, 2000
Decision Date
November 8, 2000
Product Code
LTX
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
LTX Discs, Elution

Similar 510(k) Clearances

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Other Clearances by Ab Biodisk

K Number Device Name
K081325 ETEST DORIPENEM - ANTIMICROBIAL SUSCEPTIBILITY TEST - MIC AT 0.002-32 UG/ML
K052366 ETEST TIGECYCLINE GRAM POSITIVE AND GRAM NEGATIVE AEROBIC BACTERIA, STREPTOCOCCUS SPP. AND ANAEROBIC BACTERIA
K042392 DAPTOMYCIN
K042390 ETEST FOR GEMIFLOXACIN
K040560 ETEST FOR ANTIFUNGAL SUSCEPTTIBILITY TESTING
K021445 ETEST CEFDITOREN FOR S. PNEUMONIAE AND H. INFLUENZAE
K020748 ETEST ERTAPENEM
K010363 ETEST MEROPENEM
K001547 ETEST ESBL CT/CTL STRIP; ETEST ESBL TZ/TZL STRIP
K000596 ETEST GATIFLOXACIN
Search all 64 clearances from Ab Biodisk →