Immco Diagnostics 2152-3
Immco Diagnostics 2152-3 is a Class II device made by Immco Diagnostics, Inc., cleared under FDA 510(k) K883915 on 19 Oct 1988 and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00845714001994), 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 | Number00845714001994 | Date23 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK883915 | Date19 Oct 1988 | StatusActive |
Official records
- AccessGUDID record 00845714001994
- FDA 510(k) database K883915
Across registries
- FDA 510(k) K883915 decided 19 Oct 1988 Active
- FDA GUDID UDI-DI 00845714001994 listed 23 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K883915
- Listed FDA GUDID 00845714001994
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Immco Diagnostics
- Generic name
- General specimen microscopy slide IVD, single-use
- Model / Ref / Catalog
- 2152-3
- Primary DI / UDI-DI
- 00845714001994
- 510(k) Number
- FDA product code
- DBL
- GMDN term
- General specimen microscopy slide IVD, single-use
- Device class
- Class II
- Regulation number
- 866.5660
- GUDID distribution status
- In Commercial Distribution
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