510(k) K200230

Aptiva Celiac Disease IgG Reagent by Inova Diagnostics, Inc. — Product Code MVM

K200230 is an FDA 510(k) premarket notification submitted by Inova Diagnostics, Inc. for the device "Aptiva Celiac Disease IgG Reagent". The FDA issued a decision of Substantially Equivalent on August 26, 2021. The device falls under product code MVM (Autoantibodies, Endomysial(Tissue Transglutaminase)), a Class II device regulated under 21 CFR 866.5660. Inova Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 26, 2021
Date Received
January 30, 2020
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Autoantibodies, Endomysial(Tissue Transglutaminase)
Device Class
Class II
Regulation Number
866.5660
Review Panel
IM
Submission Type