The following data is part of a premarket notification filed by Siemens Corp. with the FDA for Ur 150-ur 150t.
| Device ID | K801723 |
| 510k Number | K801723 |
| Device Name: | UR 150-UR 150T |
| Classification | Table, Cystometric, Non-electric And Accessories |
| Applicant | SIEMENS CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KQS |
| CFR Regulation Number | 876.4890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-07-24 |
| Decision Date | 1980-08-13 |