510(k) K203296

Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit by Gold Standard Diagnostics — Product Code LSR

K203296 is an FDA 510(k) premarket notification submitted by Gold Standard Diagnostics for the device "Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit". The FDA issued a decision of Substantially Equivalent on March 22, 2021. The device falls under product code LSR (Reagent, Borrelia Serological Reagent), a Class II device regulated under 21 CFR 866.3830. Gold Standard Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 22, 2021
Date Received
November 9, 2020
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Reagent, Borrelia Serological Reagent
Device Class
Class II
Regulation Number
866.3830
Review Panel
MI
Submission Type