510(k) K822785

FLUOROSET IMMUNOFLUORESCENT ANTIBODY by Immulok, Inc. — Product Code GQL

K822785 is an FDA 510(k) premarket notification submitted by Immulok, Inc. for the device "FLUOROSET IMMUNOFLUORESCENT ANTIBODY". The FDA issued a decision of Substantially Equivalent on November 29, 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
November 29, 1982
Date Received
September 14, 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