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FDA 510(k)

EASYELECTROLYTE ANALYZER AND RAPIDLYTE ANALYZER

K-Number: K000926 · 2000-05-15

ApplicantMedica Corp.
Decision Date2000-05-15
Product CodeCGZ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EASYELECTROLYTE ANALYZER AND RAPIDLYTE ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Medica Corp.. It received FDA 510(k) clearance on 2000-05-15 under 510(k) number K000926. The device is classified under product code CGZ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EASYELECTROLYTE ANALYZER AND RAPIDLYTE ANALYZER?

EASYELECTROLYTE ANALYZER AND RAPIDLYTE ANALYZER is a medical device that received FDA 510(k) clearance on 2000-05-15. The listed applicant is Medica Corp.. The 510(k) number is K000926.

When did EASYELECTROLYTE ANALYZER AND RAPIDLYTE ANALYZER receive FDA 510(k) clearance?

EASYELECTROLYTE ANALYZER AND RAPIDLYTE ANALYZER received FDA 510(k) clearance on 2000-05-15, under 510(k) number K000926.

Who is the listed applicant for EASYELECTROLYTE ANALYZER AND RAPIDLYTE ANALYZER?

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 EASYELECTROLYTE ANALYZER AND RAPIDLYTE ANALYZER?

The FDA product code for EASYELECTROLYTE ANALYZER AND RAPIDLYTE ANALYZER is CGZ.

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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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