The following data is part of a premarket notification filed by O-two Systems Intl., Inc. with the FDA for Autovent 1000.
| Device ID | K983785 |
| 510k Number | K983785 |
| Device Name: | AUTOVENT 1000 |
| Classification | Ventilator, Emergency, Powered (resuscitator) |
| Applicant | O-TWO SYSTEMS INTL., INC. 7575 KIMBEL ST., UNIT 5 MISSISSAUGA Ontario L5s 1c8, CA |
| Contact | Kevin Bowden |
| Correspondent | Kevin Bowden O-TWO SYSTEMS INTL., INC. 7575 KIMBEL ST., UNIT 5 MISSISSAUGA Ontario L5s 1c8, CA |
| Product Code | BTL |
| CFR Regulation Number | 868.5925 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-10-27 |
| Decision Date | 1998-10-29 |
| Summary: | summary |