The following data is part of a premarket notification filed by Dms Products, Inc. with the FDA for Rapidec Ur.
| Device ID | K894805 |
| 510k Number | K894805 |
| Device Name: | RAPIDEC UR |
| Classification | Kit, Screening, Urine |
| Applicant | DMS PRODUCTS, INC. DART'S MILL PROFESSIONAL VILL. RT. 523, BOX 95 Flemington, NJ 08822 |
| Contact | Janis Freestone |
| Correspondent | Janis Freestone DMS PRODUCTS, INC. DART'S MILL PROFESSIONAL VILL. RT. 523, BOX 95 Flemington, NJ 08822 |
| Product Code | JXA |
| CFR Regulation Number | 866.2660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-07-28 |
| Decision Date | 1989-09-26 |