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FDA 510(k)

ACA ETHYL ALCOHOL (ALC) ANALYTICAL TEST PACKS

K-Number: K881344 · 1989-01-24

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1989-01-24
Product CodeDIC
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ACA ETHYL ALCOHOL (ALC) ANALYTICAL TEST PACKS 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 1989-01-24 under 510(k) number K881344. 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 ACA ETHYL ALCOHOL (ALC) ANALYTICAL TEST PACKS?

ACA ETHYL ALCOHOL (ALC) ANALYTICAL TEST PACKS is a medical device that received FDA 510(k) clearance on 1989-01-24. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K881344.

When did ACA ETHYL ALCOHOL (ALC) ANALYTICAL TEST PACKS receive FDA 510(k) clearance?

ACA ETHYL ALCOHOL (ALC) ANALYTICAL TEST PACKS received FDA 510(k) clearance on 1989-01-24, under 510(k) number K881344.

Who is the listed applicant for ACA ETHYL ALCOHOL (ALC) ANALYTICAL TEST PACKS?

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 ACA ETHYL ALCOHOL (ALC) ANALYTICAL TEST PACKS?

The FDA product code for ACA ETHYL ALCOHOL (ALC) ANALYTICAL TEST PACKS 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)

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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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