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MODEL 1100 APC(ANGIOPLASTY PRESSURE CONTROLLER)

Page Type
Cleared 510(K)
510(k) Number
K853136
510(k) Type
Traditional
Applicant
E.A. FISCHIONE INSTRUMENT MFG.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/1985
Days to Decision
130 days

MODEL 1100 APC(ANGIOPLASTY PRESSURE CONTROLLER)

Page Type
Cleared 510(K)
510(k) Number
K853136
510(k) Type
Traditional
Applicant
E.A. FISCHIONE INSTRUMENT MFG.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/1985
Days to Decision
130 days