SIENET DICOM GATEWAY— 510(k) K952533
Substantially EquivalentSiemens AG
FDA 510(k) clearance K952533 for SIENET DICOM GATEWAY, Substantially Equivalent on 1995-08-23. Applicant: Siemens AG.
Clearance details
- Applicant
- Siemens AG
- Product code
- Code LMD
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Iselin, NJ, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.