The following data is part of a premarket notification filed by Becton Dickinson And Co. with the FDA for Bd Veritor System For The Rapid Detection Of Flu A + B Clia Waived Kit.
Device ID | K152870 |
510k Number | K152870 |
Device Name: | BD Veritor System For The Rapid Detection Of Flu A + B CLIA Waived Kit |
Classification | Devices Detecting Influenza A, B, And C Virus Antigens |
Applicant | BECTON DICKINSON AND CO. 10865 ROAD TO THE CURE, SUITE 200 San Diego, CA 92121 |
Contact | Gregory P. Payne |
Correspondent | Gregory P. Payne BECTON DICKINSON AND CO. 10865 ROAD TO THE CURE, SUITE 200 San Diego, CA 92121 |
Product Code | PSZ |
CFR Regulation Number | 866.3328 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-09-30 |
Decision Date | 2015-10-27 |
Summary: | summary |