MD Resource RM2000
by Medical Device Resource Corp.
MD Resource RM2000 is a Class II device made by Medical Device Resource Corp., cleared under FDA 510(k) K850704 on 24 May 1985 and listed in FDA GUDID since 13 Sep 2016 (UDI-DI 00859898006454), 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 | Number00859898006454 | Date13 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK850704 | Date24 May 1985 | StatusActive |
Official records
- AccessGUDID record 00859898006454
- FDA 510(k) database K850704
Across registries
- FDA 510(k) K850704 decided 24 May 1985 Active
- FDA GUDID UDI-DI 00859898006454 listed 13 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K850704
- Listed FDA GUDID 00859898006454
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- MD Resource
- Generic name
- Surgical suction system
- Model / Ref / Catalog
- RM2000
- Primary DI / UDI-DI
- 00859898006454
- 510(k) Number
- FDA product code
- JCX
- GMDN term
- Surgical suction system
- Device class
- Class II
- Regulation number
- 878.4780
- GUDID distribution status
- In Commercial Distribution
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