Imbio LDA 3.0.2
by Imbio, LLC
Imbio LDA 3.0.2 is a Class II device made by Imbio, LLC, cleared under FDA 510(k) K141069 on 17 Sep 2014 and listed in FDA GUDID since 23 Nov 2020 (UDI-DI 00850894007575), active as of 22 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 | Number00850894007575 | Date23 Nov 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK141069 | Date17 Sep 2014 | StatusActive |
Official records
- AccessGUDID record 00850894007575
- FDA 510(k) database K141069
Across registries
- FDA 510(k) K141069 decided 17 Sep 2014 Active
- FDA GUDID UDI-DI 00850894007575 listed 23 Nov 2020 Listed
Timeline
- Cleared FDA 510(k) K141069
- Listed FDA GUDID 00850894007575
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Imbio LDA
- Generic name
- Radiology DICOM image processing application software
- Model / reference
- 3.0.2
- Primary DI / UDI-DI
- 00850894007575
- 510(k) Number
- FDA product code
- JAK
- GMDN term
- Radiology DICOM image processing application software
- Device class
- Class II
- Regulation number
- 892.1750
- GUDID distribution status
- In Commercial Distribution
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