The following data is part of a premarket notification filed by Diatek, Inc. with the FDA for Diatek 600 Thermometer System.
| Device ID | K833568 |
| 510k Number | K833568 |
| Device Name: | DIATEK 600 THERMOMETER SYSTEM |
| Classification | Thermometer, Electronic, Clinical |
| Applicant | DIATEK, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FLL |
| CFR Regulation Number | 880.2910 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-10-12 |
| Decision Date | 1984-01-10 |