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FDA 510(k)

EASYLYTE NA/K/CL/LI ANALYZER, MODEL 2020

K-Number: K100673 · 2010-04-06

ApplicantMedica Corp.
Decision Date2010-04-06
Product CodeJGS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EASYLYTE NA/K/CL/LI ANALYZER, MODEL 2020 is the device name listed in this FDA 510(k) record. The listed applicant is Medica Corp.. It received FDA 510(k) clearance on 2010-04-06 under 510(k) number K100673. The device is classified under product code JGS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EASYLYTE NA/K/CL/LI ANALYZER, MODEL 2020?

EASYLYTE NA/K/CL/LI ANALYZER, MODEL 2020 is a medical device that received FDA 510(k) clearance on 2010-04-06. The listed applicant is Medica Corp.. The 510(k) number is K100673.

When did EASYLYTE NA/K/CL/LI ANALYZER, MODEL 2020 receive FDA 510(k) clearance?

EASYLYTE NA/K/CL/LI ANALYZER, MODEL 2020 received FDA 510(k) clearance on 2010-04-06, under 510(k) number K100673.

Who is the listed applicant for EASYLYTE NA/K/CL/LI ANALYZER, MODEL 2020?

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

What is the FDA product code for EASYLYTE NA/K/CL/LI ANALYZER, MODEL 2020?

The FDA product code for EASYLYTE NA/K/CL/LI ANALYZER, MODEL 2020 is JGS.

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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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