The following data is part of a premarket notification filed by Vickers America Medical Corp. with the FDA for Vickers Medical Model 130 Neavent-neo.
| Device ID | K791713 |
| 510k Number | K791713 |
| Device Name: | VICKERS MEDICAL MODEL 130 NEAVENT-NEO |
| Classification | Ventilator, Continuous, Facility Use |
| Applicant | VICKERS AMERICA MEDICAL CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CBK |
| CFR Regulation Number | 868.5895 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-08-27 |
| Decision Date | 1979-09-19 |