The following data is part of a premarket notification filed by Becton, Dickinson And Company with the FDA for Bd Veritor(tm) System For Rapid Detection Of Group A Strep.
Device ID | K122718 |
510k Number | K122718 |
Device Name: | BD VERITOR(TM) SYSTEM FOR RAPID DETECTION OF GROUP A STREP |
Classification | Antigens, All Groups, Streptococcus Spp. |
Applicant | Becton, Dickinson And Company 10865 ROAD TO THE CURE, SUITE 200 San Diego, CA 92121 |
Contact | Gregory P Payne |
Correspondent | Gregory P Payne Becton, Dickinson And Company 10865 ROAD TO THE CURE, SUITE 200 San Diego, CA 92121 |
Product Code | GTY |
CFR Regulation Number | 866.3740 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-09-05 |
Decision Date | 2013-02-06 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00382902560401 | K122718 | 000 |