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FDA 510(k)

MUSCLE MASTER (MEDIUM VOLTAGE STIMULATOR)

K-Number: K864284 · 1986-12-29

Decision Date1986-12-29
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

MUSCLE MASTER (MEDIUM VOLTAGE STIMULATOR) is the device name listed in this FDA 510(k) record. The listed applicant is Modern Systems Technology, Inc.. It received FDA 510(k) clearance on 1986-12-29 under 510(k) number K864284. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the MUSCLE MASTER (MEDIUM VOLTAGE STIMULATOR)?

MUSCLE MASTER (MEDIUM VOLTAGE STIMULATOR) is a medical device that received FDA 510(k) clearance on 1986-12-29. The listed applicant is Modern Systems Technology, Inc.. The 510(k) number is K864284.

When did MUSCLE MASTER (MEDIUM VOLTAGE STIMULATOR) receive FDA 510(k) clearance?

MUSCLE MASTER (MEDIUM VOLTAGE STIMULATOR) received FDA 510(k) clearance on 1986-12-29, under 510(k) number K864284.

Who is the listed applicant for MUSCLE MASTER (MEDIUM VOLTAGE STIMULATOR)?

The FDA 510(k) record lists Modern Systems Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MUSCLE MASTER (MEDIUM VOLTAGE STIMULATOR)?

The FDA product code for MUSCLE MASTER (MEDIUM VOLTAGE STIMULATOR) is IPF.

Related Clinical Trials

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.

Other records listing Modern Systems Technology, Inc. as applicant

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.

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.

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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