The following data is part of a premarket notification filed by Inspiron Corp. with the FDA for Heater, Immersion W/ Humidifier & Nebul..
| Device ID | K760037 |
| 510k Number | K760037 |
| Device Name: | HEATER, IMMERSION W/ HUMIDIFIER & NEBUL. |
| Classification | Humidifier, Respiratory Gas, (direct Patient Interface) |
| Applicant | INSPIRON CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BTT |
| CFR Regulation Number | 868.5450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-06-15 |
| Decision Date | 1976-07-16 |