SIEMENS FIO2 SENSOR— 510(k) K991884
Substantially EquivalentSiemens Medical Solutions USA, Inc.
FDA 510(k) clearance K991884 for SIEMENS FIO2 SENSOR, Substantially Equivalent on 1999-11-03. Applicant: Siemens Medical Solutions USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Siemens Medical Solutions USA, Inc.
- Product code
- Code CCL
- Device class
- Class 2
- Regulation
- 21 CFR 868.1720
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Danvers, MA, US
Recent devices under product code CCL
view allMore clearances from Siemens Medical Solutions USA, Inc.
view allAdverse events under product code CCL
product code CCL- Other
- 2
- Total
- 2
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.