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OPTI-PLAST 7F PERIPHERAL ANGIOPLASTY CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902367
510(k) Type
Traditional
Applicant
VAS-CATH, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
12/3/1990
Days to Decision
188 days

OPTI-PLAST 7F PERIPHERAL ANGIOPLASTY CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902367
510(k) Type
Traditional
Applicant
VAS-CATH, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
12/3/1990
Days to Decision
188 days