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FLOWGUARD DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013803
510(k) Type
Traditional
Applicant
BIOSONIX LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
2/13/2002
Days to Decision
90 days
Submission Type
Summary

FLOWGUARD DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013803
510(k) Type
Traditional
Applicant
BIOSONIX LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
2/13/2002
Days to Decision
90 days
Submission Type
Summary