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IOTEC TROCAR AND FLEXIBLE CANNULA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970888
510(k) Type
Traditional
Applicant
Iotec Industries
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1998
Days to Decision
304 days
Submission Type
Summary

IOTEC TROCAR AND FLEXIBLE CANNULA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970888
510(k) Type
Traditional
Applicant
Iotec Industries
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1998
Days to Decision
304 days
Submission Type
Summary