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GALIX PACESTAR

Page Type
Cleared 510(K)
510(k) Number
K023080
510(k) Type
Traditional
Applicant
GALIX BIOMEDICAL INSTRUMENTATION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/2003
Days to Decision
267 days
Submission Type
Statement

GALIX PACESTAR

Page Type
Cleared 510(K)
510(k) Number
K023080
510(k) Type
Traditional
Applicant
GALIX BIOMEDICAL INSTRUMENTATION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/2003
Days to Decision
267 days
Submission Type
Statement