The following data is part of a premarket notification filed by Cellavision Ab with the FDA for Cellavision Dm96 Automatic Hematology Analyzer.
| Device ID | K033840 |
| 510k Number | K033840 |
| Device Name: | CELLAVISION DM96 AUTOMATIC HEMATOLOGY ANALYZER |
| Classification | Device, Automated Cell-locating |
| Applicant | CELLAVISION AB 6740 RIVERVIEW TERRACE Minneapolis, MN 55432 |
| Contact | Constance G Bundy |
| Correspondent | Constance G Bundy CELLAVISION AB 6740 RIVERVIEW TERRACE Minneapolis, MN 55432 |
| Product Code | JOY |
| CFR Regulation Number | 864.5260 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-12-10 |
| Decision Date | 2004-02-10 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 07350040970201 | K033840 | 000 |