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ARTERIALFLOW SYSTEM, MODEL 32A

Page Type
Cleared 510(K)
510(k) Number
K024019
510(k) Type
Traditional
Applicant
Aircast, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2003
Days to Decision
180 days
Submission Type
Statement

ARTERIALFLOW SYSTEM, MODEL 32A

Page Type
Cleared 510(K)
510(k) Number
K024019
510(k) Type
Traditional
Applicant
Aircast, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2003
Days to Decision
180 days
Submission Type
Statement