The following data is part of a premarket notification filed by American Diagnostic Corp. with the FDA for Netilmicin Fluorescent Immunoassay.
| Device ID | K822941 |
| 510k Number | K822941 |
| Device Name: | NETILMICIN FLUORESCENT IMMUNOASSAY |
| Classification | Radioimmunoassay, Netilmicin (i-125) |
| Applicant | AMERICAN DIAGNOSTIC CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LCE |
| CFR Regulation Number | 862.3450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-10-04 |
| Decision Date | 1982-10-26 |