The following data is part of a premarket notification filed by Hudson Oxygen Therapy Sales Co. with the FDA for Port-a-bout 240.
| Device ID | K772216 |
| 510k Number | K772216 |
| Device Name: | PORT-A-BOUT 240 |
| Classification | Regulator, Pressure, Gas Cylinder |
| Applicant | HUDSON OXYGEN THERAPY SALES CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CAN |
| CFR Regulation Number | 868.2700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-12-02 |
| Decision Date | 1978-01-05 |