The following data is part of a premarket notification filed by Unoplast A/s with the FDA for Unometer 500.
| Device ID | K896732 |
| 510k Number | K896732 |
| Device Name: | UNOMETER 500 |
| Classification | Urinometer, Mechanical |
| Applicant | UNOPLAST A/S DK-3390 HUNDESTED Denmark, DK |
| Contact | Erik Andersen |
| Correspondent | Erik Andersen UNOPLAST A/S DK-3390 HUNDESTED Denmark, DK |
| Product Code | EXR |
| CFR Regulation Number | 876.1800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-11-30 |
| Decision Date | 1990-11-02 |