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URETERAL DILATOR/SHEATH SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852793
510(k) Type
Traditional
Applicant
AMERICAN EDWARDS LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1985
Days to Decision
39 days

URETERAL DILATOR/SHEATH SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852793
510(k) Type
Traditional
Applicant
AMERICAN EDWARDS LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1985
Days to Decision
39 days