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FDA 510(k)

DUPONT ACA ION SELECTIVE ELECTRODE

K-Number: K800016 · 1980-01-21

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1980-01-21
Product CodeCEM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DUPONT ACA ION SELECTIVE ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. It received FDA 510(k) clearance on 1980-01-21 under 510(k) number K800016. 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 DUPONT ACA ION SELECTIVE ELECTRODE?

DUPONT ACA ION SELECTIVE ELECTRODE is a medical device that received FDA 510(k) clearance on 1980-01-21. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K800016.

When did DUPONT ACA ION SELECTIVE ELECTRODE receive FDA 510(k) clearance?

DUPONT ACA ION SELECTIVE ELECTRODE received FDA 510(k) clearance on 1980-01-21, under 510(k) number K800016.

Who is the listed applicant for DUPONT ACA ION SELECTIVE ELECTRODE?

The FDA 510(k) record lists E.I. Dupont DE Nemours & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUPONT ACA ION SELECTIVE ELECTRODE?

The FDA product code for DUPONT ACA ION SELECTIVE ELECTRODE is CEM.

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Other records listing E.I. Dupont DE Nemours & Co., Inc. as applicant

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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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