The following data is part of a premarket notification filed by Wako Chemicals, Usa, Inc. with the FDA for Wako Insulin Test.
| Device ID | K823939 |
| 510k Number | K823939 |
| Device Name: | WAKO INSULIN TEST |
| Classification | Radioimmunoassay, Immunoreactive Insulin |
| Applicant | WAKO CHEMICALS, USA, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CFP |
| CFR Regulation Number | 862.1405 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-12-29 |
| Decision Date | 1983-01-28 |