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CEFOTETAN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC

Page Type
Cleared 510(K)
510(k) Number
K971631
510(k) Type
Traditional
Applicant
OXOID, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
7/3/1997
Days to Decision
62 days
Submission Type
Statement

CEFOTETAN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC

Page Type
Cleared 510(K)
510(k) Number
K971631
510(k) Type
Traditional
Applicant
OXOID, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
7/3/1997
Days to Decision
62 days
Submission Type
Statement