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FDA 510(k)

BIO-STYM 250 (MUSCLE STIMULATOR)

K-Number: K891987 · 1990-01-04

ApplicantElectronic Health Technologies, Inc.
Decision Date1990-01-04
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BIO-STYM 250 (MUSCLE STIMULATOR) is the device name listed in this FDA 510(k) record. The listed applicant is Electronic Health Technologies, Inc.. It received FDA 510(k) clearance on 1990-01-04 under 510(k) number K891987. 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 BIO-STYM 250 (MUSCLE STIMULATOR)?

BIO-STYM 250 (MUSCLE STIMULATOR) is a medical device that received FDA 510(k) clearance on 1990-01-04. The listed applicant is Electronic Health Technologies, Inc.. The 510(k) number is K891987.

When did BIO-STYM 250 (MUSCLE STIMULATOR) receive FDA 510(k) clearance?

BIO-STYM 250 (MUSCLE STIMULATOR) received FDA 510(k) clearance on 1990-01-04, under 510(k) number K891987.

Who is the listed applicant for BIO-STYM 250 (MUSCLE STIMULATOR)?

The FDA 510(k) record lists Electronic Health Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIO-STYM 250 (MUSCLE STIMULATOR)?

The FDA product code for BIO-STYM 250 (MUSCLE STIMULATOR) is 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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