The following data is part of a premarket notification filed by Baxter Diagnostics, Inc. with the FDA for Microdilution/loracarbef Panels.
| Device ID | K942089 |
| 510k Number | K942089 |
| Device Name: | MICRODILUTION/LORACARBEF PANELS |
| Classification | Manual Antimicrobial Susceptibility Test Systems |
| Applicant | BAXTER DIAGNOSTICS, INC. 2040 ENTERPRISE BLVD. W. Sacramento, CA 95691 |
| Contact | Elaine K Cataplane |
| Correspondent | Elaine K Cataplane BAXTER DIAGNOSTICS, INC. 2040 ENTERPRISE BLVD. W. Sacramento, CA 95691 |
| Product Code | JWY |
| CFR Regulation Number | 866.1640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-05-02 |
| Decision Date | 1995-01-09 |