510(k) K915892

CMV IGG ELISA TEST by Gull Laboratories, Inc. — Product Code LFZ

K915892 is an FDA 510(k) premarket notification submitted by Gull Laboratories, Inc. for the device "CMV IGG ELISA TEST". The FDA issued a decision of Substantially Equivalent on February 14, 1992. The device falls under product code LFZ (Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus), a Class II device regulated under 21 CFR 866.3175. Gull Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 14, 1992
Date Received
December 24, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus
Device Class
Class II
Regulation Number
866.3175
Review Panel
MI
Submission Type