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FDA 510(k)

ACUPUNCTURE INSOLES

K-Number: K840995 · 1984-03-27

ApplicantLu LU Enterprise Co. , Ltd.
Decision Date1984-03-27
Product CodeBWK
DecisionSubstantially Equivalent

Device Summary

ACUPUNCTURE INSOLES is the device name listed in this FDA 510(k) record. The listed applicant is Lu LU Enterprise Co. , Ltd.. It received FDA 510(k) clearance on 1984-03-27 under 510(k) number K840995. The device is classified under product code BWK. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACUPUNCTURE INSOLES?

ACUPUNCTURE INSOLES is a medical device that received FDA 510(k) clearance on 1984-03-27. The listed applicant is Lu LU Enterprise Co. , Ltd.. The 510(k) number is K840995.

When did ACUPUNCTURE INSOLES receive FDA 510(k) clearance?

ACUPUNCTURE INSOLES received FDA 510(k) clearance on 1984-03-27, under 510(k) number K840995.

Who is the listed applicant for ACUPUNCTURE INSOLES?

The FDA 510(k) record lists Lu LU Enterprise Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACUPUNCTURE INSOLES?

The FDA product code for ACUPUNCTURE INSOLES is BWK.

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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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