510(k) K941924

ELVIS HSV by Diagnostic Hybrids, Inc. — Product Code GQN

K941924 is an FDA 510(k) premarket notification submitted by Diagnostic Hybrids, Inc. for the device "ELVIS HSV". The FDA issued a decision of Substantially Equivalent on May 1, 1995. The device falls under product code GQN (Antigen, Cf (Including Cf Control), Herpesvirus Hominis 1,2), a Class II device regulated under 21 CFR 866.3305. Diagnostic Hybrids, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 1, 1995
Date Received
April 20, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antigen, Cf (Including Cf Control), Herpesvirus Hominis 1,2
Device Class
Class II
Regulation Number
866.3305
Review Panel
MI
Submission Type