Immco Diagnostics 2200
Immco Diagnostics 2200 is a Class II device made by Immco Diagnostics, Inc., cleared under FDA 510(k) K060157 on 25 May 2006 (9 earlier submissions) and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00845714003318), active as of 23 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 | Number00845714003318 | Date23 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK060157 | Date25 May 2006 | StatusActive |
Official records
- AccessGUDID record 00845714003318
- FDA 510(k) database K060157
- FDA 510(k) database K982898
- FDA 510(k) database K913360
- FDA 510(k) database K912551
- FDA 510(k) database K891098
- FDA 510(k) database K891099
- FDA 510(k) database K884400
- FDA 510(k) database K883883
- FDA 510(k) database K883949
- FDA 510(k) database K883915
Across registries
- FDA 510(k) K060157 decided 25 May 2006 Active
- FDA GUDID UDI-DI 00845714003318 listed 23 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K883883
- Cleared FDA 510(k) K883949
- Cleared FDA 510(k) K884400
- Cleared FDA 510(k) K891098
- Cleared FDA 510(k) K891099
- Cleared FDA 510(k) K912551
- Cleared FDA 510(k) K913360
- Cleared FDA 510(k) K982898
- Cleared FDA 510(k) K060157
- Listed FDA GUDID 00845714003318
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Immco Diagnostics
- Generic name
- Immunohistochemistry negative control (normal animal serum) IVD
- Model / Ref / Catalog
- 2200
- Primary DI / UDI-DI
- 00845714003318
- FDA product code
- DBL, LKJ, MOB, DHN
- GMDN term
- Immunohistochemistry negative control (normal animal serum) IVD
- Device class
- Class II
- Regulation number
- 866.5660, 866.5100
- GUDID distribution status
- In Commercial Distribution
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