OMNI OXYGEN SYSTEM, MODEL 1000— 510(k) K013931
Substantially EquivalentSequal Technologies, Inc.
FDA 510(k) clearance K013931 for OMNI OXYGEN SYSTEM, MODEL 1000, Substantially Equivalent on 2002-03-27. Applicant: Sequal Technologies, Inc.. Device class: 2.
Clearance details
- Applicant
- Sequal Technologies, Inc.
- Product code
- 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
- San Diego, CA, US
Recent devices under product code CAW
view allMore clearances from Sequal Technologies, Inc.
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.