Last synced on 20 December 2024 at 11:05 pm

SURGI-VISION URETHRAL COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002345
510(k) Type
Traditional
Applicant
SURGI-VISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2000
Days to Decision
70 days
Submission Type
Summary

SURGI-VISION URETHRAL COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002345
510(k) Type
Traditional
Applicant
SURGI-VISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2000
Days to Decision
70 days
Submission Type
Summary