Vessel Occluder
by Cordis Corp.
510(k) K800074
Vessel Occluder is a medical device (FDA Class I; FDA product code GDJ, Clamp, Surgical, General & Plastic Surgery) made by Cordis Corp., cleared under FDA 510(k) K800074 on 28 Jan 1980, 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 | NumberK800074 | Date28 Jan 1980 | StatusActive |
Official records
- FDA 510(k) database K800074
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- GDJ
- Device class
- Class I
- Regulation
- 21 CFR Part 878.4800
- Advisory committee
- General, Plastic Surgery
- FDA decision
- SESE Substantially Equivalent
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