510(k) K955361

INCSTAR CYTOMEGALOVIRUS IGG ELISA ASSAY by Incstar Corp. — Product Code LFZ

K955361 is an FDA 510(k) premarket notification submitted by Incstar Corp. for the device "INCSTAR CYTOMEGALOVIRUS IGG ELISA ASSAY". The FDA issued a decision of Substantially Equivalent on July 22, 1996. The device falls under product code LFZ (Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus), a Class II device regulated under 21 CFR 866.3175. Incstar Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 22, 1996
Date Received
November 22, 1995
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