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FDA 510(k)

ELECTRONIC MUSCLE STIMULATOR

K-Number: K844489 · 1985-03-05

ApplicantBeverly Hills Exercise Equipment
Decision Date1985-03-05
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ELECTRONIC MUSCLE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Beverly Hills Exercise Equipment. It received FDA 510(k) clearance on 1985-03-05 under 510(k) number K844489. 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 ELECTRONIC MUSCLE STIMULATOR?

ELECTRONIC MUSCLE STIMULATOR is a medical device that received FDA 510(k) clearance on 1985-03-05. The listed applicant is Beverly Hills Exercise Equipment. The 510(k) number is K844489.

When did ELECTRONIC MUSCLE STIMULATOR receive FDA 510(k) clearance?

ELECTRONIC MUSCLE STIMULATOR received FDA 510(k) clearance on 1985-03-05, under 510(k) number K844489.

Who is the listed applicant for ELECTRONIC MUSCLE STIMULATOR?

The FDA 510(k) record lists Beverly Hills Exercise Equipment as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRONIC MUSCLE STIMULATOR?

The FDA product code for ELECTRONIC MUSCLE STIMULATOR is IPF.

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Related Devices (Code: IPF)

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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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