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FDA 510(k)

GEM Premier 5000 (Measured Parameters:Glucose, Lactate and Total Bilirubin)

K-Number: K160402 · 2016-12-14

ApplicantInstrumentation Laboratory CO
Decision Date2016-12-14
Product CodeCGA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GEM Premier 5000 (Measured Parameters:Glucose, Lactate and Total Bilirubin) is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 2016-12-14 under 510(k) number K160402. The device is classified under product code CGA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GEM Premier 5000 (Measured Parameters:Glucose, Lactate and Total Bilirubin)?

GEM Premier 5000 (Measured Parameters:Glucose, Lactate and Total Bilirubin) is a medical device that received FDA 510(k) clearance on 2016-12-14. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K160402.

When did GEM Premier 5000 (Measured Parameters:Glucose, Lactate and Total Bilirubin) receive FDA 510(k) clearance?

GEM Premier 5000 (Measured Parameters:Glucose, Lactate and Total Bilirubin) received FDA 510(k) clearance on 2016-12-14, under 510(k) number K160402.

Who is the listed applicant for GEM Premier 5000 (Measured Parameters:Glucose, Lactate and Total Bilirubin)?

The FDA 510(k) record lists Instrumentation Laboratory CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GEM Premier 5000 (Measured Parameters:Glucose, Lactate and Total Bilirubin)?

The FDA product code for GEM Premier 5000 (Measured Parameters:Glucose, Lactate and Total Bilirubin) is CGA.

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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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