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ELECTROSURGICAL PROBES AND DEVICES-GELTX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002269
510(k) Type
Traditional
Applicant
Ximed/Prosure/Injectx
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/2001
Days to Decision
162 days
Submission Type
Statement

ELECTROSURGICAL PROBES AND DEVICES-GELTX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002269
510(k) Type
Traditional
Applicant
Ximed/Prosure/Injectx
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/2001
Days to Decision
162 days
Submission Type
Statement