EV1000 Evecl
EV1000 Evecl is a Class II device made by Edwards Lifesciences LLC, cleared under FDA 510(k) K160552 on 1 Jun 2016 (1 earlier submission) and listed in FDA GUDID since 3 Sep 2016 (UDI-DI 00690103190366), active as of 22 Oct 2026. One FDA recall is linked to it.
Active
510(k)
Valid until
No expiry
FDA recalls
None ongoingDocuments
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00690103190366 | Date3 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK160552 | Date1 Jun 2016 | StatusActive |
Official records
- AccessGUDID record 00690103190366
- FDA 510(k) database K160552
- FDA 510(k) database K131892
Across registries
- FDA 510(k) K160552 decided 1 Jun 2016 Active
- FDA GUDID UDI-DI 00690103190366 listed 3 Sep 2016 Listed
Recalls
-
- Terminated Z-1193-2019
Potential for an electrical short circuit leading to possible fire hazard due to liquid ingress into AC power outlets.
Timeline
- Cleared FDA 510(k) K131892
- Cleared FDA 510(k) K160552
- Listed FDA GUDID 00690103190366
- Recall initiated FDA recalls Z-1193-2019
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- EV1000
- Generic name
- Electrical-only medical device connection cable, reusable
- Model / Ref / Catalog
- EVECL
- Primary DI / UDI-DI
- 00690103190366
- FDA product code
- DXG, DSB, DXN
- GMDN term
- Electrical-only medical device connection cable, reusable
- Device class
- Class II
- Regulation number
- 870.1435, 870.2770, 870.1130
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 15 Feet
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