The following data is part of a premarket notification filed by Airlife, Inc. with the FDA for Tempo2-i Disposable Thermometers.
| Device ID | K790890 |
| 510k Number | K790890 |
| Device Name: | TEMPO2-I DISPOSABLE THERMOMETERS |
| Classification | Thermometer, Clinical Color Change |
| Applicant | AIRLIFE, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | FQZ |
| CFR Regulation Number | 880.2900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-05-07 |
| Decision Date | 1979-06-27 |