The following data is part of a premarket notification filed by Beckman Coulter, Inc. with the FDA for Coulter Act 5diff Al Hematology Analyzer.
| Device ID | K032013 |
| 510k Number | K032013 |
| Device Name: | COULTER ACT 5DIFF AL HEMATOLOGY ANALYZER |
| Classification | Counter, Differential Cell |
| Applicant | BECKMAN COULTER, INC. 11800 SW 147TH AVE. M/S 31-B06 Miami, FL 33196 -2500 |
| Contact | Lourdes Coba |
| Correspondent | Lourdes Coba BECKMAN COULTER, INC. 11800 SW 147TH AVE. M/S 31-B06 Miami, FL 33196 -2500 |
| Product Code | GKZ |
| CFR Regulation Number | 864.5220 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-06-30 |
| Decision Date | 2003-07-24 |
| Summary: | summary |