OEC 9800 E/CV+ DIGITAL MOBILE IMAGING SYSTEM— 510(k) K024012
Substantially EquivalentGe Oec Medical Systems
FDA 510(k) clearance K024012 for OEC 9800 E/CV+ DIGITAL MOBILE IMAGING SYSTEM, Substantially Equivalent on 2003-03-20. Applicant: Ge Oec Medical Systems.
Clearance details
- Applicant
- Ge Oec Medical Systems
- Product code
- Code JAA
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Salt Lake City, UT, US
Adverse events under product code JAA
product code JAA- Other
- 1
- Total
- 1
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.