510(k) K821567

IMMULOK CULTURESET by Immulok, Inc. — Product Code GQL

K821567 is an FDA 510(k) premarket notification submitted by Immulok, Inc. for the device "IMMULOK CULTURESET". The FDA issued a decision of Substantially Equivalent on June 25, 1982. The device falls under product code GQL (Antisera, Fluorescent, Herpesvirus Hominis 1,2), a Class II device regulated under 21 CFR 866.3305. Immulok, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 25, 1982
Date Received
May 25, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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