The following data is part of a premarket notification filed by Dlp, Inc. with the FDA for Dispossable Suction Tube, 6 French.
| Device ID | K791846 |
| 510k Number | K791846 |
| Device Name: | DISPOSSABLE SUCTION TUBE, 6 FRENCH |
| Classification | Sucker, Cardiotomy Return, Cardiopulmonary Bypass |
| Applicant | DLP, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DTS |
| CFR Regulation Number | 870.4420 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-09-19 |
| Decision Date | 1979-10-02 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20613994698357 | K791846 | 000 |
| 20613994698333 | K791846 | 000 |
| 20613994698319 | K791846 | 000 |
| 20613994698296 | K791846 | 000 |
| 20613994698272 | K791846 | 000 |
| 20613994570448 | K791846 | 000 |