The following data is part of a premarket notification filed by Biomerieux, Inc. with the FDA for Vitek 2 Compact.
| Device ID | K050002 |
| 510k Number | K050002 |
| Device Name: | VITEK 2 COMPACT |
| Classification | System, Test, Automated, Antimicrobial Susceptibility, Short Incubation |
| Applicant | BIOMERIEUX, INC. 595 ANGLUM DR. Hazelwood, MO 63042 -2320 |
| Contact | Nancy Weaver |
| Correspondent | Nancy Weaver BIOMERIEUX, INC. 595 ANGLUM DR. Hazelwood, MO 63042 -2320 |
| Product Code | LON |
| CFR Regulation Number | 866.1645 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-01-03 |
| Decision Date | 2005-02-17 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 03573026220624 | K050002 | 000 |
| 03573026147167 | K050002 | 000 |
| 03573026136796 | K050002 | 000 |
| 03573026136789 | K050002 | 000 |
| 03573026220631 | K050002 | 000 |
| 03573026147501 | K050002 | 000 |
| 03573026147495 | K050002 | 000 |