The following data is part of a premarket notification filed by Snyder Laboratories, Inc. with the FDA for Catheters, Greenline Suction.
| Device ID | K790606 |
| 510k Number | K790606 |
| Device Name: | CATHETERS, GREENLINE SUCTION |
| Classification | Catheters, Suction, Tracheobronchial |
| Applicant | SNYDER LABORATORIES, INC. 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 | 1979-03-29 |
| Decision Date | 1979-04-23 |