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Rusch Endotracheal Tubes (Reinforced); Rusch Endotracheal Tubes (Safety Clear); Rusch Endotracheal Tubes (Safety Clear Pediatric)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241451
510(k) Type
Traditional
Applicant
Teleflex Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2025
Days to Decision
265 days
Submission Type
Summary

Rusch Endotracheal Tubes (Reinforced); Rusch Endotracheal Tubes (Safety Clear); Rusch Endotracheal Tubes (Safety Clear Pediatric)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241451
510(k) Type
Traditional
Applicant
Teleflex Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2025
Days to Decision
265 days
Submission Type
Summary