The following data is part of a premarket notification filed by Intl. Diagnostic Technology with the FDA for Fiax 100 Fluorometer.
| Device ID | K843356 |
| 510k Number | K843356 |
| Device Name: | FIAX 100 FLUOROMETER |
| Classification | Fluorometer |
| Applicant | INTL. DIAGNOSTIC TECHNOLOGY 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JZT |
| CFR Regulation Number | 866.4520 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-08-27 |
| Decision Date | 1984-09-17 |