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FDA 510(k)

NOVA II SODIUM/POTASSIUM/LITHIUM ANALYZER

K-Number: K863438 · 1986-09-29

ApplicantNova Biomedical Corp.
Decision Date1986-09-29
Product CodeJJP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

NOVA II SODIUM/POTASSIUM/LITHIUM ANALYZER 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 1986-09-29 under 510(k) number K863438. The device is classified under product code JJP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVA II SODIUM/POTASSIUM/LITHIUM ANALYZER?

NOVA II SODIUM/POTASSIUM/LITHIUM ANALYZER is a medical device that received FDA 510(k) clearance on 1986-09-29. The listed applicant is Nova Biomedical Corp.. The 510(k) number is K863438.

When did NOVA II SODIUM/POTASSIUM/LITHIUM ANALYZER receive FDA 510(k) clearance?

NOVA II SODIUM/POTASSIUM/LITHIUM ANALYZER received FDA 510(k) clearance on 1986-09-29, under 510(k) number K863438.

Who is the listed applicant for NOVA II SODIUM/POTASSIUM/LITHIUM ANALYZER?

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 NOVA II SODIUM/POTASSIUM/LITHIUM ANALYZER?

The FDA product code for NOVA II SODIUM/POTASSIUM/LITHIUM ANALYZER is JJP.

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Other records listing Nova Biomedical Corp. as applicant

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Related Devices (Code: JJP)

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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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