Last synced on 25 November 2022 at 11:04 pm

URETERO-RENOSCOPE, MODEL 8706.402, INSERTION SHEATH, MODEL 8706.042

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990050
510(k) Type
Traditional
Applicant
RICHARD WOLF MEDICAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/1999
Days to Decision
78 days
Submission Type
Summary

URETERO-RENOSCOPE, MODEL 8706.402, INSERTION SHEATH, MODEL 8706.042

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990050
510(k) Type
Traditional
Applicant
RICHARD WOLF MEDICAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/1999
Days to Decision
78 days
Submission Type
Summary