COLORVIEW 860 OR SSD-860 PULSE ECHO/MODIFICATION— 510(k) K871490
Substantially EquivalentGe Medical Systems Information Technologies
FDA 510(k) clearance K871490 for COLORVIEW 860 OR SSD-860 PULSE ECHO/MODIFICATION, Substantially Equivalent on 1987-12-07. Applicant: Ge Medical Systems Information Technologies. Device class: 2.
Clearance details
- Applicant
- Ge Medical Systems Information Technologies
- Product code
- Code DPW
- Device class
- Class 2
- Regulation
- 21 CFR 870.2100
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wallingford, CT, US
Recent devices under product code DPW
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