The following data is part of a premarket notification filed by Toa Medical Electronics Usa, Inc. with the FDA for Sysmex(tm) R-3000 Automated Reticulocyte Analyzer.
| Device ID | K912494 |
| 510k Number | K912494 |
| Device Name: | SYSMEX(TM) R-3000 AUTOMATED RETICULOCYTE ANALYZER |
| Classification | Counter, Cell, Automated (particle Counter) |
| Applicant | TOA MEDICAL ELECTRONICS USA, INC. 4410 CERRITOS AVE. Los Alamitos, CA 90720 |
| Contact | Adele Shoustal |
| Correspondent | Adele Shoustal TOA MEDICAL ELECTRONICS USA, INC. 4410 CERRITOS AVE. Los Alamitos, CA 90720 |
| Product Code | GKL |
| CFR Regulation Number | 864.5200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-06-05 |
| Decision Date | 1991-09-10 |