510(k) K181464

LIAISON Helicobacter Antigen, LIAISON Helicobacter Antigen Control Set by DiaSorin, Inc. — Product Code LYR

K181464 is an FDA 510(k) premarket notification submitted by DiaSorin, Inc. for the device "LIAISON Helicobacter Antigen, LIAISON Helicobacter Antigen Control Set". The FDA issued a decision of Substantially Equivalent on August 31, 2018. The device falls under product code LYR (Helicobacter Pylori), a Class I device regulated under 21 CFR 866.3110. DiaSorin, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 31, 2018
Date Received
June 4, 2018
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Helicobacter Pylori
Device Class
Class I
Regulation Number
866.3110
Review Panel
MI
Submission Type