The following data is part of a premarket notification filed by Hycor Biomedical, Inc. with the FDA for Hycor Hy.tec/manual Rf Auto-antibody.
| Device ID | K962729 |
| 510k Number | K962729 |
| Device Name: | HYCOR HY.TEC/MANUAL RF AUTO-ANTIBODY |
| Classification | System, Test, Rheumatoid Factor |
| Applicant | HYCOR BIOMEDICAL, INC. 7272 CHAPMAN AVE. Garden Grove, CA 92841 |
| Contact | Mehdi Alem, Ph.d. |
| Correspondent | Mehdi Alem, Ph.d. 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 | 1996-07-01 |
| Decision Date | 1997-03-07 |