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FDA 510(k)

DEMAND ETHYL ALCOHOL

K-Number: K854130 · 1985-11-05

ApplicantCooper Biomedical, Inc.
Decision Date1985-11-05
Product CodeDIC
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

DEMAND ETHYL ALCOHOL is the device name listed in this FDA 510(k) record. The listed applicant is Cooper Biomedical, Inc.. It received FDA 510(k) clearance on 1985-11-05 under 510(k) number K854130. 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 DEMAND ETHYL ALCOHOL?

DEMAND ETHYL ALCOHOL is a medical device that received FDA 510(k) clearance on 1985-11-05. The listed applicant is Cooper Biomedical, Inc.. The 510(k) number is K854130.

When did DEMAND ETHYL ALCOHOL receive FDA 510(k) clearance?

DEMAND ETHYL ALCOHOL received FDA 510(k) clearance on 1985-11-05, under 510(k) number K854130.

Who is the listed applicant for DEMAND ETHYL ALCOHOL?

The FDA 510(k) record lists Cooper Biomedical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEMAND ETHYL ALCOHOL?

The FDA product code for DEMAND ETHYL ALCOHOL is DIC.

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Other records listing Cooper Biomedical, Inc. as applicant

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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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