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FDA 510(k)

DUPONT LINEARIZATION MODULE

K-Number: K832746 · 1983-11-25

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1983-11-25
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DUPONT LINEARIZATION MODULE 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 1983-11-25 under 510(k) number K832746. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUPONT LINEARIZATION MODULE?

DUPONT LINEARIZATION MODULE is a medical device that received FDA 510(k) clearance on 1983-11-25. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K832746.

When did DUPONT LINEARIZATION MODULE receive FDA 510(k) clearance?

DUPONT LINEARIZATION MODULE received FDA 510(k) clearance on 1983-11-25, under 510(k) number K832746.

Who is the listed applicant for DUPONT LINEARIZATION MODULE?

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 LINEARIZATION MODULE?

The FDA product code for DUPONT LINEARIZATION MODULE is JQP.

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

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Related Devices (Code: JQP)

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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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