Immco Diagnostics 2302-60
Immco Diagnostics 2302-60 is a Class II device made by Immco Diagnostics, Inc., cleared under FDA 510(k) K883949 on 27 Oct 1988 and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00845714004339), 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 | Number00845714004339 | Date23 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK883949 | Date27 Oct 1988 | StatusActive |
Official records
- AccessGUDID record 00845714004339
- FDA 510(k) database K883949
Across registries
- FDA 510(k) K883949 decided 27 Oct 1988 Active
- FDA GUDID UDI-DI 00845714004339 listed 23 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K883949
- Listed FDA GUDID 00845714004339
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Immco Diagnostics
- Generic name
- Buffered sample diluent IVD
- Model / Ref / Catalog
- 2302-60
- Primary DI / UDI-DI
- 00845714004339
- 510(k) Number
- FDA product code
- LKJ
- GMDN term
- Buffered sample diluent IVD
- Device class
- Class II
- Regulation number
- 866.5100
- GUDID distribution status
- In Commercial Distribution
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