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Bendit21 Microcatheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203842
510(k) Type
Traditional
Applicant
Bend It Technologies Ltd
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
4/13/2022
Days to Decision
468 days
Submission Type
Summary

Bendit21 Microcatheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203842
510(k) Type
Traditional
Applicant
Bend It Technologies Ltd
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
4/13/2022
Days to Decision
468 days
Submission Type
Summary