The following data is part of a premarket notification filed by Medix Biotech, Inc. with the FDA for Medix Biotech Lh Enzyme Immunoassay Test Kit.
| Device ID | K873668 |
| 510k Number | K873668 |
| Device Name: | MEDIX BIOTECH LH ENZYME IMMUNOASSAY TEST KIT |
| Classification | Radioimmunoassay, Luteinizing Hormone |
| Applicant | MEDIX BIOTECH, INC. 420 LINCOLN CENTRE DR. Foster City, CA 94404 |
| Contact | John J Huang |
| Correspondent | John J Huang MEDIX BIOTECH, INC. 420 LINCOLN CENTRE DR. Foster City, CA 94404 |
| Product Code | CEP |
| CFR Regulation Number | 862.1485 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-09-10 |
| Decision Date | 1987-10-07 |