Cordia Cmv
by Cordis Corp.
510(k) K823123
Cordia Cmv is a Class II device made by Cordis Corp., cleared under FDA 510(k) K823123 on 28 Dec 1982, active as of 10 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 | NumberK823123 | Date28 Dec 1982 | StatusActive |
Official records
- FDA 510(k) database K823123
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LFZ
- Device class
- Class II
- Regulation
- 21 CFR Part 866.3175
- Advisory committee
- Microbiology
- FDA decision
- SESE Substantially Equivalent
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