The following data is part of a premarket notification filed by Beckman Coulter, Inc. with the FDA for Coulter Body Fluid Control.
| Device ID | K082162 |
| 510k Number | K082162 |
| Device Name: | COULTER BODY FLUID CONTROL |
| Classification | Mixture, Hematology Quality Control |
| 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 | JPK |
| CFR Regulation Number | 864.8625 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-07-31 |
| Decision Date | 2009-02-03 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 15099590233808 | K082162 | 000 |