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. Device class: 1.
Clearance details
- Applicant
- GE Medical Systems
- Product code
- Code DWS
- Device class
- Class 1
- Regulation
- 21 CFR 870.4500
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Palm Harbor, FL, US
Recent devices under product code DWS
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