The following data is part of a premarket notification filed by Volu Sol Medical Industries with the FDA for Elvi 840 Aggregometer.
| Device ID | K791577 |
| 510k Number | K791577 |
| Device Name: | ELVI 840 AGGREGOMETER |
| Classification | System, Automated Platelet Aggregation |
| Applicant | VOLU SOL MEDICAL INDUSTRIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JOZ |
| CFR Regulation Number | 864.5700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-08-17 |
| Decision Date | 1979-09-17 |