MODIFICATION OF VENTURI VENTILATOR— 510(k) K990429
Substantially Equivalent - Subject to Tracking Reg.Cardiopulmonary Corp.
FDA 510(k) clearance K990429 for MODIFICATION OF VENTURI VENTILATOR, Substantially Equivalent - Subject to Tracking Reg. on 1999-02-24. Applicant: Cardiopulmonary Corp..
Clearance details
- Applicant
- Cardiopulmonary Corp.
- Product code
- Code CBK
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent - Subject to Tracking Reg.
- Clearance type
- Special
- Location
- Milford, CT, US
Adverse events under product code CBK
product code CBK- Death
- 736
- Injury
- 3,628
- Malfunction
- 98,786
- Other
- 4
- Total
- 103,154
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.