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ACRON MC MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K991774
510(k) Type
Traditional
Applicant
GC AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/1999
Days to Decision
45 days
Submission Type
Statement

ACRON MC MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K991774
510(k) Type
Traditional
Applicant
GC AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/1999
Days to Decision
45 days
Submission Type
Statement