BONHAWA Respiratory Humidifier— 510(k) K223863
Substantially EquivalentTelesair, Inc.
FDA 510(k) clearance K223863 for BONHAWA Respiratory Humidifier, Substantially Equivalent on 2023-10-13. Applicant: Telesair, Inc..
Clearance details
- Applicant
- Telesair, Inc.
- Product code
- Code BTT
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
Adverse events under product code BTT
product code BTT- Death
- 60
- Injury
- 152
- Malfunction
- 7,232
- Other
- 2
- Total
- 7,446
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.