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ANGIOPLASTY BALLOON INFLATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K880158
510(k) Type
Traditional
Applicant
L.O.N. RESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1988
Days to Decision
69 days

ANGIOPLASTY BALLOON INFLATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K880158
510(k) Type
Traditional
Applicant
L.O.N. RESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1988
Days to Decision
69 days