Last synced on 25 January 2026 at 3:41 am

ELECTROSURGICAL PROBE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963901
510(k) Type
Traditional
Applicant
Smith & Nephew Endoscopy, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/1996
Days to Decision
38 days
Submission Type
Summary

ELECTROSURGICAL PROBE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963901
510(k) Type
Traditional
Applicant
Smith & Nephew Endoscopy, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/1996
Days to Decision
38 days
Submission Type
Summary