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STARION CAUTERY HOOK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000296
510(k) Type
Traditional
Applicant
STARION INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2000
Days to Decision
36 days
Submission Type
Summary

STARION CAUTERY HOOK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000296
510(k) Type
Traditional
Applicant
STARION INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2000
Days to Decision
36 days
Submission Type
Summary