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THERMAL CAUTERY PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050308
510(k) Type
Special
Applicant
STARION INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2005
Days to Decision
17 days
Submission Type
Summary

THERMAL CAUTERY PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050308
510(k) Type
Special
Applicant
STARION INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2005
Days to Decision
17 days
Submission Type
Summary