Phantom 2550-1
Phantom 2550-1 (IM-K2550-1) is a Class II device made by Innovative Med, Inc., cleared under FDA 510(k) K895761 on 18 Oct 1989 and listed in FDA GUDID since 19 Sep 2016 (UDI-DI 00851314007045), 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 | Number00851314007045 | Date19 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK895761 | Date18 Oct 1989 | StatusActive |
Official records
- AccessGUDID record 00851314007045
- FDA 510(k) database K895761
Across registries
- FDA 510(k) K895761 decided 18 Oct 1989 Active
- FDA GUDID UDI-DI 00851314007045 listed 19 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K895761
- Listed FDA GUDID 00851314007045
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Phantom
- Generic name
- General-purpose surgical suction system, vacuum
- Model / Ref / Catalog
- 2550-1, IM-K2550-1
- Primary DI / UDI-DI
- 00851314007045
- 510(k) Number
- FDA product code
- JCX
- GMDN term
- General-purpose surgical suction system, vacuum
- Device class
- Class II
- Regulation number
- 878.4780
- GUDID distribution status
- In Commercial Distribution
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