MD Resource AV2000D
by Medical Device Resource Corp.
MD Resource AV2000D is a Class I device made by Medical Device Resource Corp., cleared under FDA 510(k) K092284 on 1 Sep 2009 and listed in FDA GUDID since 8 Sep 2016 (UDI-DI 00859898006409), 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 | Number00859898006409 | Date8 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK092284 | Date1 Sep 2009 | StatusActive |
Official records
- AccessGUDID record 00859898006409
- FDA 510(k) database K092284
Across registries
- FDA 510(k) K092284 decided 1 Sep 2009 Active
- FDA GUDID UDI-DI 00859898006409 listed 8 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K092284
- Listed FDA GUDID 00859898006409
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- MD Resource
- Generic name
- Surgical suction system collection container, single-use
- Model / Ref / Catalog
- AV2000D
- Primary DI / UDI-DI
- 00859898006409
- 510(k) Number
- FDA product code
- KYZ, MUU
- GMDN term
- Surgical suction system collection container, single-use
- Device class
- Class I
- Regulation number
- 880.6960, 878.5040
- GUDID distribution status
- In Commercial Distribution
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