The following data is part of a premarket notification filed by Landmark Plastics with the FDA for Cannula, Larriat.
| Device ID | K760551 |
| 510k Number | K760551 |
| Device Name: | CANNULA, LARRIAT |
| Classification | Cannula, Nasal, Oxygen |
| Applicant | LANDMARK PLASTICS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CAT |
| CFR Regulation Number | 868.5340 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-08-30 |
| Decision Date | 1976-09-05 |