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FDA 510(k)

PARAAMAX CHLORIDE DETERMINATION BY ISE

K-Number: K854651 · 1985-12-13

ApplicantAmerican Dade
Decision Date1985-12-13
Product CodeCGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PARAAMAX CHLORIDE DETERMINATION BY ISE is the device name listed in this FDA 510(k) record. The listed applicant is American Dade. It received FDA 510(k) clearance on 1985-12-13 under 510(k) number K854651. The device is classified under product code CGJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARAAMAX CHLORIDE DETERMINATION BY ISE?

PARAAMAX CHLORIDE DETERMINATION BY ISE is a medical device that received FDA 510(k) clearance on 1985-12-13. The listed applicant is American Dade. The 510(k) number is K854651.

When did PARAAMAX CHLORIDE DETERMINATION BY ISE receive FDA 510(k) clearance?

PARAAMAX CHLORIDE DETERMINATION BY ISE received FDA 510(k) clearance on 1985-12-13, under 510(k) number K854651.

Who is the listed applicant for PARAAMAX CHLORIDE DETERMINATION BY ISE?

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

What is the FDA product code for PARAAMAX CHLORIDE DETERMINATION BY ISE?

The FDA product code for PARAAMAX CHLORIDE DETERMINATION BY ISE is CGJ.

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Related Devices (Code: CGJ)

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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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