MOBILAIRE V & III PRO2 OXYGEN SENSORS FEATURES— 510(k) K924818
Substantially EquivalentInvacare Corp.
FDA 510(k) clearance K924818 for MOBILAIRE V & III PRO2 OXYGEN SENSORS FEATURES, Substantially Equivalent on 1993-08-06. Applicant: Invacare Corp.. Device class: 2.
Clearance details
- Applicant
- Invacare Corp.
- Product code
- Product code CAW
- Device class
- Class 2
- Regulation
- 21 CFR 868.5440
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Elyria, OH, US
Recent devices under product code CAW
view allMore clearances from Invacare Corp.
view allAdverse events under product code CAW
product code CAW- Death
- 204
- Injury
- 573
- Malfunction
- 1,400
- Other
- 6
- Total
- 2,183
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.