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OPTICALLY CLEAR RADIOPAQUE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K893546
510(k) Type
Traditional
Applicant
CRITIKON COMPANY,LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/1989
Days to Decision
174 days

OPTICALLY CLEAR RADIOPAQUE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K893546
510(k) Type
Traditional
Applicant
CRITIKON COMPANY,LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/1989
Days to Decision
174 days