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CLEAR SHOT ANGIOPLASTY BALLOON INFLATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K884481
510(k) Type
Traditional
Applicant
MALLINCKROOT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1989
Days to Decision
80 days

CLEAR SHOT ANGIOPLASTY BALLOON INFLATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K884481
510(k) Type
Traditional
Applicant
MALLINCKROOT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1989
Days to Decision
80 days