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BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K894944
510(k) Type
Traditional
Applicant
PERIPHERAL SYSTEMS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1990
Days to Decision
169 days

BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K894944
510(k) Type
Traditional
Applicant
PERIPHERAL SYSTEMS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1990
Days to Decision
169 days