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UNICATH FAMILY

Page Type
Cleared 510(K)
510(k) Number
K942503
510(k) Type
Traditional
Applicant
ANGIOGRAPHIC DEVICES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/1994
Days to Decision
55 days
Submission Type
Statement

UNICATH FAMILY

Page Type
Cleared 510(K)
510(k) Number
K942503
510(k) Type
Traditional
Applicant
ANGIOGRAPHIC DEVICES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/1994
Days to Decision
55 days
Submission Type
Statement