510(k) K831343

CMV RQ BIO-ENZABEAD KIT by Litton Bionetics — Product Code LFZ

K831343 is an FDA 510(k) premarket notification submitted by Litton Bionetics for the device "CMV RQ BIO-ENZABEAD KIT". The FDA issued a decision of Substantially Equivalent on August 8, 1983. The device falls under product code LFZ (Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus), a Class II device regulated under 21 CFR 866.3175. Litton Bionetics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 8, 1983
Date Received
April 25, 1983
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