Dolphin IQ
by Viasonix Ltd
Dolphin IQ, a general-purpose ultrasound imaging system (FDA Class II) made by Viasonix Ltd, was cleared under FDA 510(k) K170859 on 14 Nov 2017 and listed in FDA GUDID on 17 Dec 2017 (UDI-DI 07290016880045); the registry lists it as not in commercial distribution (GUDID) as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number07290016880045 | Date17 Dec 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK170859 | Date14 Nov 2017 | StatusActive |
Official records
- AccessGUDID record 07290016880045
- FDA 510(k) database K170859
Across registries
- FDA 510(k) K170859 decided 14 Nov 2017 Active
- FDA GUDID UDI-DI 07290016880045 listed 17 Dec 2017 Listed
Timeline
- Cleared FDA 510(k) K170859
- Listed FDA GUDID 07290016880045
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Dolphin
- Generic name
- General-purpose ultrasound imaging system
- Model / reference
- IQ
- Primary DI / UDI-DI
- 07290016880045
- 510(k) Number
- FDA product code
- ITX, IYN
- GMDN term
- General-purpose ultrasound imaging system
- Device class
- Class II
- Regulation number
- 892.1570, 892.1550
- GUDID distribution status
- Not in Commercial Distribution
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