The following data is part of a premarket notification filed by Hycor Biomedical, Inc. with the FDA for Hytec Automimmune Kit (rf).
| Device ID | K954892 |
| 510k Number | K954892 |
| Device Name: | HYTEC AUTOMIMMUNE KIT (RF) |
| Classification | System, Test, Rheumatoid Factor |
| Applicant | HYCOR BIOMEDICAL, INC. 7272 CHAPMAN AVE. Garden Grove, CA 92841 |
| Contact | Thomas M Li |
| Correspondent | Thomas M Li HYCOR BIOMEDICAL, INC. 7272 CHAPMAN AVE. Garden Grove, CA 92841 |
| Product Code | DHR |
| CFR Regulation Number | 866.5775 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-10-25 |
| Decision Date | 1995-12-26 |