Aview Lcs 1.0
Aview Lcs 1.0 is a radiological PACS-dedicated management software (FDA Class II) made by Coreline Soft Co., Ltd., cleared under FDA 510(k) K193220 on 5 May 2020 and listed in FDA GUDID since 9 Aug 2021 (UDI-DI 08800025300039), active 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 | Number08800025300039 | Date9 Aug 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK193220 | Date5 May 2020 | StatusActive |
Official records
- AccessGUDID record 08800025300039
- FDA 510(k) database K193220
Across registries
- FDA 510(k) K193220 decided 5 May 2020 Active
- FDA GUDID UDI-DI 08800025300039 listed 9 Aug 2021 Listed
Timeline
- Cleared FDA 510(k) K193220
- Listed FDA GUDID 08800025300039
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Aview Lcs
- Generic name
- Radiological PACS-dedicated management software
- Model / reference
- 1.0
- Primary DI / UDI-DI
- 08800025300039
- 510(k) Number
- FDA product code
- LLZ, JAK
- GMDN term
- Radiological PACS-dedicated management software
- Device class
- Class II
- Regulation number
- 892.2050, 892.1750
- GUDID distribution status
- In Commercial Distribution
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