The following data is part of a premarket notification filed by Burron Medical Products, Inc. with the FDA for Cat 3040.
| Device ID | K830193 |
| 510k Number | K830193 |
| Device Name: | CAT 3040 |
| Classification | Container, I.v. |
| Applicant | BURRON MEDICAL PRODUCTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KPE |
| CFR Regulation Number | 880.5025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-01-20 |
| Decision Date | 1983-03-09 |