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PERCUPRO MESSENGER BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K094048
510(k) Type
Traditional
Applicant
Cardiosolutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/2011
Days to Decision
560 days
Submission Type
Summary

PERCUPRO MESSENGER BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K094048
510(k) Type
Traditional
Applicant
Cardiosolutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/2011
Days to Decision
560 days
Submission Type
Summary