510(k) K883399

UBI MAGIWEL CMV IGG QUANTITATIVE by United Biotech, Inc. — Product Code LFZ

K883399 is an FDA 510(k) premarket notification submitted by United Biotech, Inc. for the device "UBI MAGIWEL CMV IGG QUANTITATIVE". The FDA issued a decision of Substantially Equivalent on March 27, 1989. The device falls under product code LFZ (Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus), a Class II device regulated under 21 CFR 866.3175. United Biotech, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 27, 1989
Date Received
August 11, 1988
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