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ANGIOFLOW METER, ANGIOFLOW ANTEGRADE CATHETER, ANGIOFLOW RETROGRADE CATHETER, MODELS HVT100, ADT1001, ADT1002

Page Type
Cleared 510(K)
510(k) Number
K033424
510(k) Type
Special
Applicant
Transonic Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2003
Days to Decision
49 days
Submission Type
Summary

ANGIOFLOW METER, ANGIOFLOW ANTEGRADE CATHETER, ANGIOFLOW RETROGRADE CATHETER, MODELS HVT100, ADT1001, ADT1002

Page Type
Cleared 510(K)
510(k) Number
K033424
510(k) Type
Special
Applicant
Transonic Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2003
Days to Decision
49 days
Submission Type
Summary