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FDA 510(k)

Lumipulse G LH Calibrators

K-Number: K163521 · 2017-01-12

ApplicantFujirebio Diagnostics,Inc.
Decision Date2017-01-12
Product CodeJIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

Lumipulse G LH Calibrators is a medical device manufactured by Fujirebio Diagnostics,Inc.. It received FDA 510(k) clearance on 2017-01-12 under approval number K163521. The device is classified under product code JIT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Lumipulse G LH Calibrators?

Lumipulse G LH Calibrators is a medical device that received FDA 510(k) clearance on 2017-01-12. It is manufactured by Fujirebio Diagnostics,Inc.. The 510(k) number is K163521.

When was Lumipulse G LH Calibrators approved by the FDA?

Lumipulse G LH Calibrators received FDA 510(k) clearance on 2017-01-12, under approval number K163521.

What company makes Lumipulse G LH Calibrators?

Lumipulse G LH Calibrators is manufactured by Fujirebio Diagnostics,Inc..

What is the FDA product code for Lumipulse G LH Calibrators?

The FDA product code for Lumipulse G LH Calibrators is JIT.

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Related Devices (Code: JIT)

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Official Source

View on FDA Database →

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

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