FDA 510(k)

EGS MODEL 300

K-Number: K832371 · 1983-10-06

ApplicantElectro-Med Health Industries, Inc.

Decision Date1983-10-06

Product Code

DecisionSubstantially Equivalent

Device Summary

EGS MODEL 300 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 1983-10-06 under 510(k) number K832371. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EGS MODEL 300?

EGS MODEL 300 is a medical device that received FDA 510(k) clearance on 1983-10-06. The listed applicant is Electro-Med Health Industries, Inc.. The 510(k) number is K832371.

When did EGS MODEL 300 receive FDA 510(k) clearance?

EGS MODEL 300 received FDA 510(k) clearance on 1983-10-06, under 510(k) number K832371.

Who is the listed applicant for EGS MODEL 300?

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

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Other records listing Electro-Med Health Industries, Inc. as applicant

K852077VERSA STIM 380, MUSCLE STIMULATOR K832803STEAM PAK MOIST HEAT K832804SESAM TABLE K832370EGS MODEL 100-2 K802107EGS #300 BATTERY OPER. PORTA. MUSCLE STI

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.