The following data is part of a premarket notification filed by Technicon Instruments Corp. with the FDA for Rdw Parameter For The Technicon H6000.
| Device ID | K834026 |
| 510k Number | K834026 |
| Device Name: | RDW PARAMETER FOR THE TECHNICON H6000 |
| Classification | Counter, Cell, Automated (particle Counter) |
| Applicant | TECHNICON INSTRUMENTS CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GKL |
| CFR Regulation Number | 864.5200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-11-22 |
| Decision Date | 1984-01-30 |