Last synced on 2 December 2022 at 11:04 pm

URETERAL DILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852324
510(k) Type
Traditional
Applicant
AMERICAN EDWARDS LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1985
Days to Decision
83 days

URETERAL DILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852324
510(k) Type
Traditional
Applicant
AMERICAN EDWARDS LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1985
Days to Decision
83 days