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AMCATH URETERAL DILATORS MODELS 7100,7110,7120

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894925
510(k) Type
Traditional
Applicant
INTEC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/1989
Days to Decision
133 days

AMCATH URETERAL DILATORS MODELS 7100,7110,7120

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894925
510(k) Type
Traditional
Applicant
INTEC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/1989
Days to Decision
133 days