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FDA 510(k)

LECTROSTILL DISTILLED WATER U.S.P.

K-Number: K854764 · 1985-12-30

ApplicantElectrified Companies, Inc.
Decision Date1985-12-30
Product Code
DecisionSubstantially Equivalent

Device Summary

LECTROSTILL DISTILLED WATER U.S.P. is the device name listed in this FDA 510(k) record. The listed applicant is Electrified Companies, Inc.. It received FDA 510(k) clearance on 1985-12-30 under 510(k) number K854764. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LECTROSTILL DISTILLED WATER U.S.P.?

LECTROSTILL DISTILLED WATER U.S.P. is a medical device that received FDA 510(k) clearance on 1985-12-30. The listed applicant is Electrified Companies, Inc.. The 510(k) number is K854764.

When did LECTROSTILL DISTILLED WATER U.S.P. receive FDA 510(k) clearance?

LECTROSTILL DISTILLED WATER U.S.P. received FDA 510(k) clearance on 1985-12-30, under 510(k) number K854764.

Who is the listed applicant for LECTROSTILL DISTILLED WATER U.S.P.?

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

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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