510(k) K982027

MODIFICATION TO COPALIS CMV TOTAL ANTIBODY ASSAY by DiaSorin, Inc. — Product Code LFZ

K982027 is an FDA 510(k) premarket notification submitted by DiaSorin, Inc. for the device "MODIFICATION TO COPALIS CMV TOTAL ANTIBODY ASSAY". The FDA issued a decision of Substantially Equivalent on November 25, 1998. The device falls under product code LFZ (Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus), a Class II device regulated under 21 CFR 866.3175. DiaSorin, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 25, 1998
Date Received
June 2, 1998
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