K241451
- 510(k) number
- K241451
- Device name
- Rusch Endotracheal Tubes (Reinforced); Rusch Endotracheal Tubes (Safety Clear); Rusch Endotracheal Tubes (Safety Clear Pediatric)
- Applicant
- Teleflex Incorporated NC · US
- Product code
- BTR — Tube, Tracheal (W/Wo Connector)
- Decision date
- 2025-02-11
- Date received
- 2024-05-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K241451.pdf
Official FDA record: K241451
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.