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 |