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The Signature Series Magnum 100

by Progressive Electrical Therapeutics

510(k) K934919

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 NumberK934919 Date6 Apr 1994ClearedStatusActive

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  • Withdrawn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, 23 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 device is a physical medicine device, as indicated by its advisory committee classification and device type. It is identified as THE SIGNATURE SERIES, MAGNUM 100, a product manufactured by Progressive Electrical Therapeutics.

It received FDA 510(k) clearance under K934919 on April 6, 1994, with a traditional clearance pathway and a substantially equivalent decision. The device is authorized for marketing in the United States, with the manufacturer located in Nevada, Missouri.

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Questions

AI-generated answers, 23 Sep 2026

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

  • What is THE SIGNATURE SERIES, MAGNUM 100 used for?

    THE SIGNATURE SERIES, MAGNUM 100 is a physical medicine device, as classified by its advisory committee and device type, intended for use in physical medicine applications based on its FDA 510(k) clearance.

  • Who manufactures THE SIGNATURE SERIES, MAGNUM 100 and where are they located?

    THE SIGNATURE SERIES, MAGNUM 100 is manufactured by Progressive Electrical Therapeutics, located at 200 S. Alma, Nevada, Missouri 64772, United States.

  • What regulatory clearance does THE SIGNATURE SERIES, MAGNUM 100 have and when was it granted?

    THE SIGNATURE SERIES, MAGNUM 100 received FDA 510(k) clearance under K934919 on April 6, 1994, through a traditional clearance pathway with a substantially equivalent decision.