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SMASH PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CARDIOVASCULAR DEVICES PANEL

Page Type
Cleared 510(K)
510(k) Number
K972512
510(k) Type
Traditional
Applicant
BOSTON SCIENTIFIC SCIMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1998
Days to Decision
220 days
Submission Type
Summary

SMASH PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CARDIOVASCULAR DEVICES PANEL

Page Type
Cleared 510(K)
510(k) Number
K972512
510(k) Type
Traditional
Applicant
BOSTON SCIENTIFIC SCIMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1998
Days to Decision
220 days
Submission Type
Summary