Last synced on 25 January 2026 at 3:41 am

MICROENDOSCOPE(8755.401,411,461,451)/EXTERNAL SHEATH(8755.221,222)/VERESS CANNULA(8755.211,212)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971420
510(k) Type
Traditional
Applicant
Richard Wolf Medical Instruments Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/1997
Days to Decision
188 days
Submission Type
Summary

MICROENDOSCOPE(8755.401,411,461,451)/EXTERNAL SHEATH(8755.221,222)/VERESS CANNULA(8755.211,212)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971420
510(k) Type
Traditional
Applicant
Richard Wolf Medical Instruments Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/1997
Days to Decision
188 days
Submission Type
Summary