G.E. STERILE DIGITAL ANGIOGRAPHIC TRAY— 510(k) K960143
UnknownGE Medical Systems
FDA 510(k) clearance K960143 for G.E. STERILE DIGITAL ANGIOGRAPHIC TRAY, Unknown on 1996-04-09. Applicant: GE Medical Systems.
Clearance details
- Applicant
- GE Medical Systems
- Product code
- Code DWS
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Palm Harbor, FL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.