The following data is part of a premarket notification filed by Bivona Medical Technologies with the FDA for Bivona Carden Intermittent Jetting Device.
| Device ID | K895946 |
| 510k Number | K895946 |
| Device Name: | BIVONA CARDEN INTERMITTENT JETTING DEVICE |
| Classification | Ventilator, Emergency, Powered (resuscitator) |
| Applicant | BIVONA MEDICAL TECHNOLOGIES 5700 WEST 23RD AVE. Gary, IN 46406 |
| Contact | Harry M Kaufman |
| Correspondent | Harry M Kaufman BIVONA MEDICAL TECHNOLOGIES 5700 WEST 23RD AVE. Gary, IN 46406 |
| Product Code | BTL |
| CFR Regulation Number | 868.5925 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-10-11 |
| Decision Date | 1990-01-09 |