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FUTREX-6100/XL

Page Type
Cleared 510(K)
510(k) Number
K963271
510(k) Type
Traditional
Applicant
FUTREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/1998
Days to Decision
729 days
Submission Type
Statement

FUTREX-6100/XL

Page Type
Cleared 510(K)
510(k) Number
K963271
510(k) Type
Traditional
Applicant
FUTREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/1998
Days to Decision
729 days
Submission Type
Statement