The following data is part of a premarket notification filed by Respiratory Care, Inc. with the FDA for A Quapak.
| Device ID | K811073 |
| 510k Number | K811073 |
| Device Name: | A QUAPAK |
| Classification | Humidifier, Respiratory Gas, (direct Patient Interface) |
| Applicant | RESPIRATORY CARE, INC. 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 | 1981-04-20 |
| Decision Date | 1981-04-29 |