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FDA 510(k)

MEASURE-UP MUSCLE STIMULATOR

K-Number: K831003 · 1983-06-20

ApplicantMeasure-Up Intl., Inc.
Decision Date1983-06-20
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MEASURE-UP MUSCLE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Measure-Up Intl., Inc.. It received FDA 510(k) clearance on 1983-06-20 under 510(k) number K831003. 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 MEASURE-UP MUSCLE STIMULATOR?

MEASURE-UP MUSCLE STIMULATOR is a medical device that received FDA 510(k) clearance on 1983-06-20. The listed applicant is Measure-Up Intl., Inc.. The 510(k) number is K831003.

When did MEASURE-UP MUSCLE STIMULATOR receive FDA 510(k) clearance?

MEASURE-UP MUSCLE STIMULATOR received FDA 510(k) clearance on 1983-06-20, under 510(k) number K831003.

Who is the listed applicant for MEASURE-UP MUSCLE STIMULATOR?

The FDA 510(k) record lists Measure-Up Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEASURE-UP MUSCLE STIMULATOR?

The FDA product code for MEASURE-UP MUSCLE STIMULATOR 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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