The following data is part of a premarket notification filed by Dade Behring, Inc. with the FDA for Dade Behring Labpro Alert Software System.
| Device ID | K070346 |
| 510k Number | K070346 |
| Device Name: | DADE BEHRING LABPRO ALERT SOFTWARE SYSTEM |
| Classification | System, Test, Automated, Antimicrobial Susceptibility, Short Incubation |
| Applicant | DADE BEHRING, INC. 2040 ENTERPRISE BLVD. West Sacramento, CA 95691 |
| Contact | Robert Eusebio |
| Correspondent | Robert Eusebio DADE BEHRING, INC. 2040 ENTERPRISE BLVD. West Sacramento, CA 95691 |
| Product Code | LON |
| CFR Regulation Number | 866.1645 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-02-06 |
| Decision Date | 2007-07-18 |
| Summary: | summary |