510(k) K862705

CYTOMEGALOVIRUS IGG EIA TEST KIT by Labsystems, Inc. — Product Code GQI

K862705 is an FDA 510(k) premarket notification submitted by Labsystems, Inc. for the device "CYTOMEGALOVIRUS IGG EIA TEST KIT". The FDA issued a decision of Substantially Equivalent on October 1, 1986. The device falls under product code GQI (Antiserum, Cf, Cytomegalovirus), a Class II device regulated under 21 CFR 866.3175. Labsystems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 1, 1986
Date Received
July 16, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antiserum, Cf, Cytomegalovirus
Device Class
Class II
Regulation Number
866.3175
Review Panel
MI
Submission Type