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FDA 510(k)

HAWKINS ELECTROKINETIC BODY ACTIVATING

K-Number: K820938 · 1982-06-11

ApplicantLeisure Way
Decision Date1982-06-11
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HAWKINS ELECTROKINETIC BODY ACTIVATING is the device name listed in this FDA 510(k) record. The listed applicant is Leisure Way. It received FDA 510(k) clearance on 1982-06-11 under 510(k) number K820938. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAWKINS ELECTROKINETIC BODY ACTIVATING?

HAWKINS ELECTROKINETIC BODY ACTIVATING is a medical device that received FDA 510(k) clearance on 1982-06-11. The listed applicant is Leisure Way. The 510(k) number is K820938.

When did HAWKINS ELECTROKINETIC BODY ACTIVATING receive FDA 510(k) clearance?

HAWKINS ELECTROKINETIC BODY ACTIVATING received FDA 510(k) clearance on 1982-06-11, under 510(k) number K820938.

Who is the listed applicant for HAWKINS ELECTROKINETIC BODY ACTIVATING?

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

What is the FDA product code for HAWKINS ELECTROKINETIC BODY ACTIVATING?

The FDA product code for HAWKINS ELECTROKINETIC BODY ACTIVATING is IPF.

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Related Devices (Code: IPF)

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

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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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