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FDA 510(k)

DUPONT DIMENSION(R) ETHYL ALCOHOL(ALC) METHOD

K-Number: K904302 · 1990-10-12

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1990-10-12
Product CodeDIC
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

DUPONT DIMENSION(R) ETHYL ALCOHOL(ALC) METHOD 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 1990-10-12 under 510(k) number K904302. The device is classified under product code DIC. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUPONT DIMENSION(R) ETHYL ALCOHOL(ALC) METHOD?

DUPONT DIMENSION(R) ETHYL ALCOHOL(ALC) METHOD is a medical device that received FDA 510(k) clearance on 1990-10-12. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K904302.

When did DUPONT DIMENSION(R) ETHYL ALCOHOL(ALC) METHOD receive FDA 510(k) clearance?

DUPONT DIMENSION(R) ETHYL ALCOHOL(ALC) METHOD received FDA 510(k) clearance on 1990-10-12, under 510(k) number K904302.

Who is the listed applicant for DUPONT DIMENSION(R) ETHYL ALCOHOL(ALC) METHOD?

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 DIMENSION(R) ETHYL ALCOHOL(ALC) METHOD?

The FDA product code for DUPONT DIMENSION(R) ETHYL ALCOHOL(ALC) METHOD is DIC.

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

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Related Devices (Code: DIC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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