ZIEHM VISION RFD— 510(k) K132904
Substantially EquivalentZiehm Imaging GmbH
FDA 510(k) clearance K132904 for ZIEHM VISION RFD, Substantially Equivalent on 2013-12-05. Applicant: Ziehm Imaging GmbH.
Clearance details
- Applicant
- Ziehm Imaging GmbH
- Product code
- Code JAA
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Orlando, FL, 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.