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FDA 510(k)

ETHYL CHLORIDE DISPENSER

K-Number: K984564 · 1999-12-02

ApplicantDukal Corp.
Decision Date1999-12-02
Product CodeMLY
DecisionSubstantially Equivalent

Device Summary

ETHYL CHLORIDE DISPENSER is the device name listed in this FDA 510(k) record. The listed applicant is Dukal Corp.. It received FDA 510(k) clearance on 1999-12-02 under 510(k) number K984564. The device is classified under product code MLY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ETHYL CHLORIDE DISPENSER?

ETHYL CHLORIDE DISPENSER is a medical device that received FDA 510(k) clearance on 1999-12-02. The listed applicant is Dukal Corp.. The 510(k) number is K984564.

When did ETHYL CHLORIDE DISPENSER receive FDA 510(k) clearance?

ETHYL CHLORIDE DISPENSER received FDA 510(k) clearance on 1999-12-02, under 510(k) number K984564.

Who is the listed applicant for ETHYL CHLORIDE DISPENSER?

The FDA 510(k) record lists Dukal Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ETHYL CHLORIDE DISPENSER?

The FDA product code for ETHYL CHLORIDE DISPENSER is MLY.

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Other records listing Dukal Corp. as applicant

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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