The following data is part of a premarket notification filed by Armkel, Llc. with the FDA for Virogen Hsv Antibody Test.
Device ID | K871426 |
510k Number | K871426 |
Device Name: | VIROGEN HSV ANTIBODY TEST |
Classification | Antisera, Cf, Herpesvirus Hominis 1,2 |
Applicant | ARMKEL, LLC. HALF ACRE RD. P.O. BOX 1001 Cranbury, NJ 08512 |
Contact | C Kolakowsky |
Correspondent | C Kolakowsky ARMKEL, LLC. HALF ACRE RD. P.O. BOX 1001 Cranbury, NJ 08512 |
Product Code | GQO |
CFR Regulation Number | 866.3305 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-04-09 |
Decision Date | 1987-10-15 |