510(k) K852928

VIROGEN HERPES SLIDE TEST by Armkel, LLC — Product Code GQO

K852928 is an FDA 510(k) premarket notification submitted by Armkel, LLC for the device "VIROGEN HERPES SLIDE TEST". The FDA issued a decision of Substantially Equivalent on October 17, 1985. The device falls under product code GQO (Antisera, Cf, Herpesvirus Hominis 1,2), a Class II device regulated under 21 CFR 866.3305. Armkel, LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 17, 1985
Date Received
July 9, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antisera, Cf, Herpesvirus Hominis 1,2
Device Class
Class II
Regulation Number
866.3305
Review Panel
MI
Submission Type