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MODEL 1000 APC-ANGIOPLASTY PRESSURE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K841493
510(k) Type
Traditional
Applicant
E.A. FISCHIONE INSTRUMENT MFG.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/1984
Days to Decision
62 days

MODEL 1000 APC-ANGIOPLASTY PRESSURE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K841493
510(k) Type
Traditional
Applicant
E.A. FISCHIONE INSTRUMENT MFG.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/1984
Days to Decision
62 days