The following data is part of a premarket notification filed by Zeus Scientific, Inc. with the FDA for Test, (ivdp) Mitochondrial Antibody.
| Device ID | K760155 |
| 510k Number | K760155 |
| Device Name: | TEST, (IVDP) MITOCHONDRIAL ANTIBODY |
| Classification | Antimitochondrial Antibody, Indirect Immunofluorescent, Antigen, Control |
| Applicant | ZEUS SCIENTIFIC, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DBM |
| CFR Regulation Number | 866.5090 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-07-02 |
| Decision Date | 1976-07-20 |