The following data is part of a premarket notification filed by Cytotech, Inc. with the FDA for Antinuclear Antibody (ana) Positive Controls.
| Device ID | K873249 |
| 510k Number | K873249 |
| Device Name: | ANTINUCLEAR ANTIBODY (ANA) POSITIVE CONTROLS |
| Classification | Antinuclear Antibody, Antigen, Control |
| Applicant | CYTOTECH, INC. 11035 ROSELLE STREET, SUITE A San Diego, CA 92121 |
| Contact | Kiehl, Phd |
| Correspondent | Kiehl, Phd CYTOTECH, INC. 11035 ROSELLE STREET, SUITE A San Diego, CA 92121 |
| Product Code | LKJ |
| CFR Regulation Number | 866.5100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-08-17 |
| Decision Date | 1987-09-22 |