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FDA 510(k)

MEDICA EASYLYTE SODIUM/POTASSIUM ANALYZER

K-Number: K864872 · 1987-03-13

ApplicantMedica Corp.
Decision Date1987-03-13
Product CodeJGS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MEDICA EASYLYTE SODIUM/POTASSIUM 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 1987-03-13 under 510(k) number K864872. 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 MEDICA EASYLYTE SODIUM/POTASSIUM ANALYZER?

MEDICA EASYLYTE SODIUM/POTASSIUM ANALYZER is a medical device that received FDA 510(k) clearance on 1987-03-13. The listed applicant is Medica Corp.. The 510(k) number is K864872.

When did MEDICA EASYLYTE SODIUM/POTASSIUM ANALYZER receive FDA 510(k) clearance?

MEDICA EASYLYTE SODIUM/POTASSIUM ANALYZER received FDA 510(k) clearance on 1987-03-13, under 510(k) number K864872.

Who is the listed applicant for MEDICA EASYLYTE SODIUM/POTASSIUM 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 MEDICA EASYLYTE SODIUM/POTASSIUM ANALYZER?

The FDA product code for MEDICA EASYLYTE SODIUM/POTASSIUM ANALYZER is JGS.

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Other records listing Medica Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: 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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