The following data is part of a premarket notification filed by Hamilton Co. with the FDA for Digital Diluter/dispensers.
| Device ID | K822688 |
| 510k Number | K822688 |
| Device Name: | DIGITAL DILUTER/DISPENSERS |
| Classification | Station, Pipetting And Diluting, For Clinical Use |
| Applicant | HAMILTON CO. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | JQW |
| CFR Regulation Number | 862.2750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-09-03 |
| Decision Date | 1982-11-05 |