Last synced on 9 December 2022 at 11:04 pm

URETHROTOME 8667.XXX AND 8670.XXX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000905
510(k) Type
Traditional
Applicant
RICHARD WOLF MEDICAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/2000
Days to Decision
52 days
Submission Type
Summary

URETHROTOME 8667.XXX AND 8670.XXX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000905
510(k) Type
Traditional
Applicant
RICHARD WOLF MEDICAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/2000
Days to Decision
52 days
Submission Type
Summary