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

SENSITIVE HAEMOPHILUS INFLUENZAE, STREPTOCOCCUS PNEUMONIA, (HP) MIC SUSCEPTIBILITY PLATES

K Number: K093741 · Decision Feb 25, 2010
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
440
Applicant Total
7
Review Days
83

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Basic Information

Device Name
SENSITIVE HAEMOPHILUS INFLUENZAE, STREPTOCOCCUS PNEUMONIA, (HP) MIC SUSCEPTIBILITY PLATES
K Number
K093741
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.1640
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Trek Diagnostic Systems, Ltd.
Date Received
December 4, 2009
Decision Date
February 25, 2010
Product Code
JWY
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
JWY Manual Antimicrobial Susceptibility Test Systems

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JWY), ordered by most recent decision date.

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Other Clearances by Trek Diagnostic Systems, Ltd.

K Number Device Name
K110583 SENSITITRE OPTIREAD
K111429 SENSITITRE (R) HP MIC SUSCEPTIBILITY PLATE WITH CEFAROLINE (0.004-8UG/ML) AND THE SENSITITRE (R) 18-24 HOUR MIC SUSCE...
K110331 SENSITITRE AIM (TM)
K092445 SENSITITRE 18-24 HOUR SUSCEPTIBILITY PLATES
K062681 SENSITITRE HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP) MIC PLATE
K041534 SENSITITRE HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP) MIC SUSCEPTIBILITY PLATE AND SUSCEPTIBILITY TEST PANEL