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TYSHAK PERIPHERAL BALLOON DILATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K931009
510(k) Type
Traditional
Applicant
NUMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/1993
Days to Decision
305 days
Submission Type
Statement

TYSHAK PERIPHERAL BALLOON DILATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K931009
510(k) Type
Traditional
Applicant
NUMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/1993
Days to Decision
305 days
Submission Type
Statement