Combination Powered Electrical Muscle Stimulator and Interferential Stimulator, Model BMLS04-1

FDA 510(k) K041388 · Biomedical Life Systems, Inc.

Substantially Equivalent

510(k) numberK041388

Submission

Device name
Combination Powered Electrical Muscle Stimulator and Interferential Stimulator, Model BMLS04-1
Applicant
Biomedical Life Systems, Inc.
Vista, CA, US
Received
May 25, 2004
Decision date
November 23, 2004
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
GZJ – Stimulator, Nerve, Transcutaneous, For Pain Relief
Device class
Class II (moderate risk)
Regulation
21 CFR 882.5890
Specialty
Neurology

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K252236CP Relief Wand Rx - TENS/NMESGZJ · Special N & C Holdings, LLC08/15/2025SE
K232441Unipro (K-UNIPRO-US)GZJ · Traditional Tenscare, Ltd.08/30/2024SE
K241228TENSWaveGZJ · Abbreviated Zynex Medical Officer08/27/2024SE
K233046Electrical Neuromuscular Stimulator, Cure TrioGZJ · Traditional Oriental Inspiration Limited04/19/2024SE
K222879Transcutaneous Electrical Nerve Stimulator (model: TENS WMPS6-1)GZJ · Traditional Wuxi Jiajian Medical Instrument Co., Ltd.01/24/2023SE
K212618iRelieve Microcurrent Pain Relief SystemGZJ · Traditional Fast Track Technologies, Inc.09/14/2022SE
K213802StimOnTM Pain Relief System (GM2439)GZJ · Traditional Gimer Medical Co., Ltd.08/26/2022SE
K220578Transcutaneous Electrical Nerve Stimulator (Model RJTENS-1)GZJ · Traditional Bozhou Rongjian Medical Appliance Co., Ltd.05/25/2022SE

More from Bozhou Rongjian Medical Appliance Co., Ltd.

510(k)DeviceDecision
K172971BMLS16-1NUH · Traditional 07/08/2018SE
K102051Pain BuddyNUH · Traditional 07/29/2011SE
K061476Electro-Nerve Stimulator TENS, Model BMLS06-1GZJ · Traditional 07/26/2006SE
K042711Model BMLS03-7GZJ · Traditional 03/14/2005SE
K040007Interferential Stimulator, Model BMLS02-6LIH · Traditional 07/07/2004SE
K033174BMLS03-3IPF · Traditional 06/30/2004SE
K040824Interferential Stimulator, Model BMLS03-6LIH · Traditional 04/29/2004SE
K040306High Voltage Pulsed Stimulator, Model BMLS02-7IPF · Traditional 03/23/2004SE
K033455Electro-Nerve Stimulator TENS, Model BMLS03-5GZJ · Traditional 01/15/2004SE
K031427Electro Neuromuscular Stimulator, Model BMLS03-1IPF · Traditional 08/19/2003SE

Questions and answers

When was Combination Powered Electrical Muscle Stimulator and Interferential Stimulator, Model BMLS04-1 cleared by the FDA?

Combination Powered Electrical Muscle Stimulator and Interferential Stimulator, Model BMLS04-1 (K041388) received a 510(k) decision of Substantially Equivalent on November 23, 2004, 182 days after the submission was received.

What is the product code of K041388?

The FDA product code is GZJ – Stimulator, Nerve, Transcutaneous, For Pain Relief, a Class II (moderate risk) device regulated under 21 CFR 882.5890.