The following data is part of a premarket notification filed by Armkel, Llc. with the FDA for Bactigen Group B Streptococcus-cs Test.
Device ID | K872114 |
510k Number | K872114 |
Device Name: | BACTIGEN GROUP B STREPTOCOCCUS-CS TEST |
Classification | Antisera, All Groups, Streptococcus Spp. |
Applicant | ARMKEL, LLC. HALF ACRE RD. P.O. BOX 1001 Cranbury, NJ 08512 |
Contact | Anne Duff |
Correspondent | Anne Duff ARMKEL, LLC. HALF ACRE RD. P.O. BOX 1001 Cranbury, NJ 08512 |
Product Code | GTZ |
CFR Regulation Number | 866.3740 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-06-01 |
Decision Date | 1987-08-27 |