SSD-870 CARDIO VASCULAR PHASED ARRAY SECTOR SCANN.— 510(k) K880217
Substantially EquivalentGe Medical Systems Information Technologies
FDA 510(k) clearance K880217 for SSD-870 CARDIO VASCULAR PHASED ARRAY SECTOR SCANN., Substantially Equivalent on 1988-04-25. Applicant: Ge Medical Systems Information Technologies. Device class: 2.
Clearance details
- Applicant
- Ge Medical Systems Information Technologies
- Product code
- Code DXK
- Device class
- Class 2
- Regulation
- 21 CFR 870.2330
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wallingford, CT, US
Recent devices under product code DXK
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