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MODIFICATION TO SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX TV SYSTEM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020126
510(k) Type
Traditional
Applicant
SURX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/2002
Days to Decision
59 days
Submission Type
Summary

MODIFICATION TO SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX TV SYSTEM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020126
510(k) Type
Traditional
Applicant
SURX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/2002
Days to Decision
59 days
Submission Type
Summary