The following data is part of a premarket notification filed by Roche Molecular Systems, Inc. with the FDA for Cobas Cdiff Nucleic Acid Test For Use On The Cobas Liat System.
| Device ID | K212427 |
| 510k Number | K212427 |
| Device Name: | Cobas Cdiff Nucleic Acid Test For Use On The Cobas Liat System |
| Classification | C. Difficile Toxin Gene Amplification Assay |
| Applicant | Roche Molecular Systems, Inc. 4300 Hacienda Drive Pleasanton, CA 94588 -2722 |
| Contact | Kaitlyn Hameister |
| Correspondent | Kaitlyn Hameister Roche Molecular Systems, Inc. 4300 Hacienda Drive Pleasanton, CA 94588 -2722 |
| Product Code | OZN |
| CFR Regulation Number | 866.3130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2021-08-04 |
| Decision Date | 2021-10-20 |