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NCONTACT VISITRAX GUIDED COAGULATION SYSTEM KIT, MODELS CSK-212 AND CSK-515

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071819
510(k) Type
Special
Applicant
Ncontact Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2007
Days to Decision
23 days
Submission Type
Summary

NCONTACT VISITRAX GUIDED COAGULATION SYSTEM KIT, MODELS CSK-212 AND CSK-515

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071819
510(k) Type
Special
Applicant
Ncontact Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2007
Days to Decision
23 days
Submission Type
Summary