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FDA 510(k)

EGS #300 BATTERY OPER. PORTA. MUSCLE STI

K-Number: K802107 · 1980-10-03

ApplicantElectro-Med Health Industries, Inc.
Decision Date1980-10-03
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EGS #300 BATTERY OPER. PORTA. MUSCLE STI is the device name listed in this FDA 510(k) record. The listed applicant is Electro-Med Health Industries, Inc.. It received FDA 510(k) clearance on 1980-10-03 under 510(k) number K802107. 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 EGS #300 BATTERY OPER. PORTA. MUSCLE STI?

EGS #300 BATTERY OPER. PORTA. MUSCLE STI is a medical device that received FDA 510(k) clearance on 1980-10-03. The listed applicant is Electro-Med Health Industries, Inc.. The 510(k) number is K802107.

When did EGS #300 BATTERY OPER. PORTA. MUSCLE STI receive FDA 510(k) clearance?

EGS #300 BATTERY OPER. PORTA. MUSCLE STI received FDA 510(k) clearance on 1980-10-03, under 510(k) number K802107.

Who is the listed applicant for EGS #300 BATTERY OPER. PORTA. MUSCLE STI?

The FDA 510(k) record lists Electro-Med Health Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EGS #300 BATTERY OPER. PORTA. MUSCLE STI?

The FDA product code for EGS #300 BATTERY OPER. PORTA. MUSCLE STI is IPF.

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Other records listing Electro-Med Health Industries, 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.

K852077VERSA STIM 380, MUSCLE STIMULATORK832371EGS MODEL 300K832803STEAM PAK MOIST HEATK832804SESAM TABLEK832370EGS MODEL 100-2

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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