The following data is part of a premarket notification filed by Ohmeda Medical with the FDA for Ohmeda 7900 Anesthesia Ventilator.
| Device ID | K960964 |
| 510k Number | K960964 |
| Device Name: | OHMEDA 7900 ANESTHESIA VENTILATOR |
| Classification | Ventilator, Continuous, Facility Use |
| Applicant | OHMEDA MEDICAL OHMEDA DRIVE, P.O. BOX 7550 Madison, WI 53707 -7550 |
| Contact | Charles Morreale |
| Correspondent | Charles Morreale OHMEDA MEDICAL OHMEDA DRIVE, P.O. BOX 7550 Madison, WI 53707 -7550 |
| Product Code | CBK |
| CFR Regulation Number | 868.5895 [🔎] |
| Decision | Se Subject To Tracking Reg (ST) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-03-11 |
| Decision Date | 1996-09-27 |
| Summary: | summary |