The following data is part of a premarket notification filed by Ackrad Laboratories with the FDA for Bronchitrac Df Dual Resp/catheter.
| Device ID | K833633 |
| 510k Number | K833633 |
| Device Name: | BRONCHITRAC DF DUAL RESP/CATHETER |
| Classification | Catheters, Suction, Tracheobronchial |
| Applicant | ACKRAD LABORATORIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BSY |
| CFR Regulation Number | 868.6810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-10-17 |
| Decision Date | 1983-12-08 |