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TOCO LITE, MODEL TD-01

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013477
510(k) Type
Traditional
Applicant
VENTREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2002
Days to Decision
90 days
Submission Type
Summary

TOCO LITE, MODEL TD-01

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013477
510(k) Type
Traditional
Applicant
VENTREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2002
Days to Decision
90 days
Submission Type
Summary