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FDA 510(k)

Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit

K-Number: K200025 · 2020-04-06

Decision Date2020-04-06
Product CodeLSR
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit is a medical device manufactured by Gold Standard Diagnostics. It received FDA 510(k) clearance on 2020-04-06 under approval number K200025. The device is classified under product code LSR. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit?

Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit is a medical device that received FDA 510(k) clearance on 2020-04-06. It is manufactured by Gold Standard Diagnostics. The 510(k) number is K200025.

When was Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit approved by the FDA?

Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit received FDA 510(k) clearance on 2020-04-06, under approval number K200025.

What company makes Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit?

Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit is manufactured by Gold Standard Diagnostics.

What is the FDA product code for Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit?

The FDA product code for Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit is LSR.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.