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REMEL LORACARBEF 30 MCG SUSCEPTIBILITY DISK

Page Type
Cleared 510(K)
510(k) Number
K931799
510(k) Type
Traditional
Applicant
REMEL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/1993
Days to Decision
64 days
Submission Type
Statement

REMEL LORACARBEF 30 MCG SUSCEPTIBILITY DISK

Page Type
Cleared 510(K)
510(k) Number
K931799
510(k) Type
Traditional
Applicant
REMEL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/1993
Days to Decision
64 days
Submission Type
Statement