CORRIDOR4DM
by Invia
510(k) K080575
CORRIDOR4DM is a medical device (FDA Class II; FDA product code KPS, System, Tomography, Computed, Emission) made by Invia, cleared under FDA 510(k) K080575 on 13 May 2008, 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 | FDA 510(k)SESE | NumberK080575 | Date13 May 2008 | StatusActive |
Official records
- FDA 510(k) database K080575
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- KPS
- Device class
- Class II
- Regulation
- 21 CFR Part 892.1200
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
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