The following data is part of a premarket notification filed by Intl. Immunoassay Laboratories, Inc. with the FDA for Eia-f8 Enzymeimmunoassay Kit For Quant..
| Device ID | K821963 |
| 510k Number | K821963 |
| Device Name: | EIA-F8 ENZYMEIMMUNOASSAY KIT FOR QUANT. |
| Classification | Test, Qualitative And Quantitative Factor Deficiency |
| Applicant | INTL. IMMUNOASSAY LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GGP |
| CFR Regulation Number | 864.7290 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-07-01 |
| Decision Date | 1982-07-27 |