510(k) K791058

ANTIBODY TO HERPESVIRUS HOMINIS by Electro-Nucleonics Laboratories, Inc. — Product Code GQO

K791058 is an FDA 510(k) premarket notification submitted by Electro-Nucleonics Laboratories, Inc. for the device "ANTIBODY TO HERPESVIRUS HOMINIS". The FDA issued a decision of Substantially Equivalent on September 7, 1979. The device falls under product code GQO (Antisera, Cf, Herpesvirus Hominis 1,2), a Class II device regulated under 21 CFR 866.3305. Electro-Nucleonics Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 7, 1979
Date Received
June 8, 1979
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