The following data is part of a premarket notification filed by Biovation, Inc. with the FDA for Biovation Nephelometer.
| Device ID | K792045 |
| 510k Number | K792045 |
| Device Name: | BIOVATION NEPHELOMETER |
| Classification | Nephelometer, For Clinical Use |
| Applicant | BIOVATION, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JQX |
| CFR Regulation Number | 862.2700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-10-12 |
| Decision Date | 1979-10-30 |