Last synced on 14 November 2025 at 11:06 pm

VEROSCOPE OPTICAL VERESS CANNULA & DILATION TUBE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K041321
510(k) Type
Traditional
Applicant
RICHARD WOLF MEDICAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/2004
Days to Decision
52 days
Submission Type
Summary

VEROSCOPE OPTICAL VERESS CANNULA & DILATION TUBE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K041321
510(k) Type
Traditional
Applicant
RICHARD WOLF MEDICAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/2004
Days to Decision
52 days
Submission Type
Summary