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LINEZOLID ANTIMICROBIAL SUSCEPTIBILITY TEST DISC

Page Type
Cleared 510(K)
510(k) Number
K010537
510(k) Type
Traditional
Applicant
OXOID, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/24/2001
Days to Decision
60 days
Submission Type
Statement

LINEZOLID ANTIMICROBIAL SUSCEPTIBILITY TEST DISC

Page Type
Cleared 510(K)
510(k) Number
K010537
510(k) Type
Traditional
Applicant
OXOID, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/24/2001
Days to Decision
60 days
Submission Type
Statement