The following data is part of a premarket notification filed by Siemens Corp. with the FDA for Uroskop A And B.
| Device ID | K781532 |
| 510k Number | K781532 |
| Device Name: | UROSKOP A AND B |
| Classification | Table, Radiographic, Tilting |
| Applicant | SIEMENS CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IXR |
| CFR Regulation Number | 892.1980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-09-06 |
| Decision Date | 1978-09-14 |