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ANGIOPLASTY INFLATOR

Page Type
Cleared 510(K)
510(k) Number
K911295
510(k) Type
Traditional
Applicant
VASTEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/1991
Days to Decision
109 days

ANGIOPLASTY INFLATOR

Page Type
Cleared 510(K)
510(k) Number
K911295
510(k) Type
Traditional
Applicant
VASTEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/1991
Days to Decision
109 days