Corridor4DM v2017
by Invia
Corridor4DM v2017 is a medical device (FDA Class II; FDA product code LLZ, System, Image Processing, Radiological) made by Invia, cleared under FDA 510(k) K101279 on 4 Aug 2010 and listed in FDA GUDID since 8 Feb 2017 (UDI-DI 00864974000233), 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 | Number00864974000233 | Date8 Feb 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK101279 | Date4 Aug 2010 | StatusActive |
Official records
- AccessGUDID record 00864974000233
- FDA 510(k) database K101279
Across registries
- FDA 510(k) K101279 decided 4 Aug 2010 Active
- FDA GUDID UDI-DI 00864974000233 listed 8 Feb 2017 Listed
Timeline
- Cleared FDA 510(k) K101279
- Listed FDA GUDID 00864974000233
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Corridor4DM
- Generic name
- Radiology DICOM image processing application software
- Model / reference
- v2017
- Primary DI / UDI-DI
- 00864974000233
- 510(k) Number
- FDA product code
- LLZ
- GMDN term
- Radiology DICOM image processing application software
- Device class
- Class II
- Regulation number
- 892.2050
- GUDID distribution status
- In Commercial Distribution
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