The following data is part of a premarket notification filed by Medovations, Inc. with the FDA for Connecting Tubes.
| Device ID | K831007 |
| 510k Number | K831007 |
| Device Name: | CONNECTING TUBES |
| Classification | Pump, Portable, Aspiration (manual Or Powered) |
| Applicant | MEDOVATIONS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BTA |
| CFR Regulation Number | 878.4780 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-03-30 |
| Decision Date | 1983-05-18 |