The following data is part of a premarket notification filed by Hospitak, Inc. with the FDA for Disposable Temperature Probe.
| Device ID | K792426 |
| 510k Number | K792426 |
| Device Name: | DISPOSABLE TEMPERATURE PROBE |
| Classification | Thermometer, Clinical Mercury |
| Applicant | HOSPITAK, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FLK |
| CFR Regulation Number | 880.2920 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-11-28 |
| Decision Date | 1980-01-16 |