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Stimtech Neuromuscular Stimulator, C 600

by Stimulation Technology, Inc.

510(k) K791048

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK791048 Date3 Jul 1979ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
IPF
Device Class
Class II
Regulation
21 CFR Part 890.5850
Advisory Committee
Physical Medicine
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 25 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Stimtech Neuromuscular Stimulator, C 600 is a device that delivers electrical stimulation to muscles for therapeutic purposes. It is designed to stimulate muscle contractions to treat certain medical conditions. The device is classified under product code IPF and is intended for use in physical medicine applications.

The Stimtech Neuromuscular Stimulator, C 600 is supplied by Stimulation Technology, Inc. and received FDA 510(k) clearance on July 3, 1979. It is not specified as single-use or reusable, and no information regarding sterility, MRI safety, or storage conditions is provided. The device is authorized under K791048.

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