The following data is part of a premarket notification filed by Med Air Technology, Inc. with the FDA for Hy-flow Non-rebreathing Valve Assembly.
| Device ID | K871367 |
| 510k Number | K871367 |
| Device Name: | HY-FLOW NON-REBREATHING VALVE ASSEMBLY |
| Classification | Valve, Non-rebreathing |
| Applicant | MED AIR TECHNOLOGY, INC. 2519 E. KEARNEY Springfield, MO 65803 |
| Contact | Lois A Hansen |
| Correspondent | Lois A Hansen MED AIR TECHNOLOGY, INC. 2519 E. KEARNEY Springfield, MO 65803 |
| Product Code | CBP |
| CFR Regulation Number | 868.5870 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-04-07 |
| Decision Date | 1987-06-19 |