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MODIFIED NUMED BALLOON ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K883948
510(k) Type
Traditional
Applicant
NUMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/1989
Days to Decision
220 days

MODIFIED NUMED BALLOON ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K883948
510(k) Type
Traditional
Applicant
NUMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/1989
Days to Decision
220 days