The following data is part of a premarket notification filed by Kyoto Diagnostics, Inc. with the FDA for Kyotest Uk Urine Test Reagent Strip.
| Device ID | K841715 |
| 510k Number | K841715 |
| Device Name: | KYOTEST UK URINE TEST REAGENT STRIP |
| Classification | Nitroprusside, Ketones (urinary, Non-quant.) |
| Applicant | KYOTO DIAGNOSTICS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JIN |
| CFR Regulation Number | 862.1435 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-04-24 |
| Decision Date | 1984-05-31 |