The following data is part of a premarket notification filed by Baxter Diagnostics, Inc. with the FDA for Dried Gram-negative Cefpodoxime.
| Device ID | K941030 |
| 510k Number | K941030 |
| Device Name: | DRIED GRAM-NEGATIVE CEFPODOXIME |
| Classification | Panels, Test, Susceptibility, Antimicrobial |
| Applicant | BAXTER DIAGNOSTICS, INC. 2040 ENTERPRISE BLVD. W. Sacramento, CA 95691 |
| Contact | Elaine K Catapane |
| Correspondent | Elaine K Catapane BAXTER DIAGNOSTICS, INC. 2040 ENTERPRISE BLVD. W. Sacramento, CA 95691 |
| Product Code | LTT |
| CFR Regulation Number | 866.1640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-03-04 |
| Decision Date | 1995-02-16 |