BLEASE FRONTLINE GENIUS RANGE ANAESTHESIA MACHINE— 510(k) K982137
Substantially EquivalentBlease Medical Equipment , Ltd.
FDA 510(k) clearance K982137 for BLEASE FRONTLINE GENIUS RANGE ANAESTHESIA MACHINE, Substantially Equivalent on 1999-04-09. Applicant: Blease Medical Equipment , Ltd..
Clearance details
- Applicant
- Blease Medical Equipment , Ltd.
- Product code
- Code BSZ
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Orlando, FL, US
Adverse events under product code BSZ
product code BSZ- Death
- 23
- Injury
- 298
- Malfunction
- 32,987
- Total
- 33,308
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.