Last synced on 16 August 2024 at 11:05 pm

COAXIAL BALLOON URETHRAL DILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831384
510(k) Type
Traditional
Applicant
THOMAS J. FOGARTY, M.D.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/1983
Days to Decision
89 days

COAXIAL BALLOON URETHRAL DILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831384
510(k) Type
Traditional
Applicant
THOMAS J. FOGARTY, M.D.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/1983
Days to Decision
89 days