The following data is part of a premarket notification filed by Burron Medical Products, Inc. with the FDA for Ureofix 500 Urine Measuring System.
| Device ID | K813082 |
| 510k Number | K813082 |
| Device Name: | UREOFIX 500 URINE MEASURING SYSTEM |
| Classification | Device, Urine Flow Rate Measuring, Non-electrical, Disposable |
| Applicant | BURRON MEDICAL PRODUCTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FFG |
| CFR Regulation Number | 876.1800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-11-02 |
| Decision Date | 1981-12-31 |