K241339
- 510(k) number
- K241339
- Device name
- Besmed Bacterial Filter and HMEF
- Applicant
- Besmed Health Business Corp TW
- Product code
- CAH — Filter, Bacterial, Breathing-Circuit
- Decision date
- 2024-11-14
- Date received
- 2024-05-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K241339.pdf
Official FDA record: K241339
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.