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 |