The following data is part of a premarket notification filed by Hardy Diagnostics with the FDA for Granada Medium.
| Device ID | K173903 |
| 510k Number | K173903 |
| Device Name: | Granada Medium |
| Classification | Gbs Culture Media, Selective And Differential |
| Applicant | Hardy Diagnostics 1430 West McCoy Lane Santa Maria, CA 93455 |
| Contact | Rianna Malherbe |
| Correspondent | Rianna Malherbe Hardy Diagnostics 1430 West McCoy Lane Santa Maria, CA 93455 |
| Product Code | PQZ |
| CFR Regulation Number | 866.2360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-12-22 |
| Decision Date | 2018-03-22 |
| Summary: | summary |