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FDA 510(k)

ELECTRICAL MUSCLE STIMULATOR

K-Number: K820884 · 1982-04-29

ApplicantNitron Electronics
Decision Date1982-04-29
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ELECTRICAL MUSCLE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Nitron Electronics. It received FDA 510(k) clearance on 1982-04-29 under 510(k) number K820884. 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 ELECTRICAL MUSCLE STIMULATOR?

ELECTRICAL MUSCLE STIMULATOR is a medical device that received FDA 510(k) clearance on 1982-04-29. The listed applicant is Nitron Electronics. The 510(k) number is K820884.

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

ELECTRICAL MUSCLE STIMULATOR received FDA 510(k) clearance on 1982-04-29, under 510(k) number K820884.

Who is the listed applicant for ELECTRICAL MUSCLE STIMULATOR?

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

What is the FDA product code for ELECTRICAL MUSCLE STIMULATOR?

The FDA product code for ELECTRICAL 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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