The following data is part of a premarket notification filed by Hardy Diagnostics with the FDA for Hardydisk Ast Doripenem 10 Ug.
| Device ID | K080019 |
| 510k Number | K080019 |
| Device Name: | HARDYDISK AST DORIPENEM 10 UG |
| Classification | Susceptibility Test Discs, Antimicrobial |
| Applicant | HARDY DIAGNOSTICS 1430 WEST MCCOY LN. Santa Maria, CA 93455 |
| Contact | Wendy Phillips |
| Correspondent | Wendy Phillips HARDY DIAGNOSTICS 1430 WEST MCCOY LN. Santa Maria, CA 93455 |
| Product Code | JTN |
| CFR Regulation Number | 866.1620 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-01-03 |
| Decision Date | 2008-01-29 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00816576021864 | K080019 | 000 |
| 00816576021857 | K080019 | 000 |