The following data is part of a premarket notification filed by Cepheid with the FDA for Xpert Vana Assay.
| Device ID | K092953 |
| 510k Number | K092953 |
| Device Name: | XPERT VANA ASSAY |
| Classification | System, Test, Genotypic Detection, Resistant Markers, Enterococcus Species |
| Applicant | CEPHEID 904 CARIBBEAN DRIVE Sunnyvale, CA 94089 -1189 |
| Contact | Russel K Enns |
| Correspondent | Russel K Enns CEPHEID 904 CARIBBEAN DRIVE Sunnyvale, CA 94089 -1189 |
| Product Code | NIJ |
| CFR Regulation Number | 866.1640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-09-24 |
| Decision Date | 2009-12-17 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 07332940000233 | K092953 | 000 |