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FDA 510(k)

ANALYZER, SODIUM/POTASSIUM

K-Number: K791175 · 1979-08-10

ApplicantNova Biomedical Corp.
Decision Date1979-08-10
Product CodeCEM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ANALYZER, SODIUM/POTASSIUM is the device name listed in this FDA 510(k) record. The listed applicant is Nova Biomedical Corp.. It received FDA 510(k) clearance on 1979-08-10 under 510(k) number K791175. The device is classified under product code CEM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANALYZER, SODIUM/POTASSIUM?

ANALYZER, SODIUM/POTASSIUM is a medical device that received FDA 510(k) clearance on 1979-08-10. The listed applicant is Nova Biomedical Corp.. The 510(k) number is K791175.

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

ANALYZER, SODIUM/POTASSIUM received FDA 510(k) clearance on 1979-08-10, under 510(k) number K791175.

Who is the listed applicant for ANALYZER, SODIUM/POTASSIUM?

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

What is the FDA product code for ANALYZER, SODIUM/POTASSIUM?

The FDA product code for ANALYZER, SODIUM/POTASSIUM is CEM.

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Related Devices (Code: CEM)

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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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