The following data is part of a premarket notification filed by Stanco Medical, Inc. with the FDA for Right Atrial Line Kit.
| Device ID | K802287 |
| 510k Number | K802287 |
| Device Name: | RIGHT ATRIAL LINE KIT |
| Classification | Catheter, Percutaneous |
| Applicant | STANCO MEDICAL, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DQY |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-09-19 |
| Decision Date | 1980-11-20 |