(75 days)
No
The device description and intended use focus on standard electrotherapy modalities (NMES, TENS, IFS, FES) with programmable parameters and pre-set regimens. There is no mention of adaptive algorithms, learning capabilities, or any terms associated with AI/ML.
Yes
The device is described as a "multifunction electrotherapy device with various treatment modes that allow for neuromuscular electrical stimulation (NMES), transcutaneous electrical nerve stimulation (TENS), interferential current stimulation (IFS), and functional electrical stimulation (FES)" used to treat various medical conditions such as pain, muscle atrophy, and re-education, clearly indicating its therapeutic purpose.
No
The device is described as an electrotherapy device used for various stimulation therapies (NMES, TENS, IFS, FES) to treat conditions like pain, muscle issues, and gait improvement. Its purpose is therapeutic, not diagnostic.
No
The device description explicitly states it is a "battery-powered, multifunction device" with "Two independent stimulation channels" and "Two independent intensity controls," indicating it is a hardware device that delivers electrical stimulation.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In Vitro Diagnostic devices are used to examine specimens (like blood, urine, or tissue) taken from the human body to provide information for diagnosis, monitoring, or screening.
- Device Function: The 300 PV is an electrotherapy device that applies electrical stimulation to the body for therapeutic purposes (pain relief, muscle stimulation, etc.). It does not analyze samples taken from the body.
- Intended Use: The intended uses listed are all related to applying electrical stimulation for various physical conditions, not for analyzing biological samples.
Therefore, the 300 PV falls under the category of a therapeutic medical device, not an In Vitro Diagnostic device.
N/A
Intended Use / Indications for Use
The 300 PV is a multifunction electrotherapy device with various treatment modes that allow for neuromuscular electrical stimulation (NMES), transcutaneous electrical nerve stimulation (TENS), interferential current stimulation (IFS), and functional electrical stimulation (FES).
As a NMES device, the 300 PV is indicated for the following conditions:
- Retarding or preventing disuse atrophy .
- Maintaining or increasing range of motion ●
- Re-educating muscles ●
- Relaxation of muscle spasm .
- Increasing local blood circulation .
- Prevention of venous thrombosis of the calf muscles immediately after surgery .
As a TENS device, the 300 PV is indicated for the following conditions:
- Symptomatic relief and management of chronic, intractable pain .
- Adjunctive treatment for post-surgical and post-trauma acute pain .
As an IFS device, the 300 PV is indicated for the following conditions:
- Symptomatic relief of acute pain .
- Symptomatic relief and management of chronic pain .
As a FES device, the 300 PV is indicated for the following condition:
- Stimulation of the muscles in the leg and ankle of partially paralyzed patients to provide e flexion of the foot and thus improve the patient's gait.
Product codes
IPF, GZI, GZJ, LIH
Device Description
The Empi 300 PV Complete Electrotherapy System (300 PV) is a battery-powered, multifunction device intended to provide clinicians with the flexibility to prescribe multiple stimulation therapy regimens with the same device. The 300 PV offers the following features:
- Two independent stimulation channels (CH1 and CH2), each of which can provide NMES, TENS, IF, or FES therapy. HV therapy can be accomplished using CH1.
- Two independent intensity controls corresponding to each of the stimulation ● channels with a maximum stimulation of 100 mA from each channel.
- Timed therapy sessions
- Continuous or cycled stimulation
- Adjustable pulse rates
- Adjustable ON and OFF time controls
- Balanced asymmetrical and symmetrical biphasic waveforms
- Thirteen preprogrammed regimens: five for NMES; one for TENS; one for ● IF; two for HV and four that can be customized by the clinician (two NMES and two HV).
- Lock option for clinician to control treatment regimens and stimulus intensity .
- Pause button for patient to pause stimulation. During pause, the timer will ● not countdown if timing has been set up. Upon restart, the device assumes the previous treatment stimulation parameters but a stimulus intensity of zero.
- Optional external hand or foot switch used to control the device output during when used as an FES device for gait training
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Calf muscles, leg and ankle (for FES)
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Clinicians
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Not Found
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 890.5850 Powered muscle stimulator.
(a)
Identification. A powered muscle stimulator is an electrically powered device intended for medical purposes that repeatedly contracts muscles by passing electrical currents through electrodes contacting the affected body area.(b)
Classification. Class II (performance standards).
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KO21100 1013
510(k) Summary
for
300 PV Complete Electrotherapy System
1. SPONSOR
Empi 599 Cardigan Road St. Paul, Minnesota 55126-4099
Contact Person: John Buan (651) 415-9000 Telephone:
April 2, 2002 Date Prepared:
2. DEVICE NAME
| Proprietary Name: | 300 PV Complete Electrotherapy System |
|---|---|
| Common/Usual Name: | Electrical Muscle and Nerve Stimulator |
| Classification Names: | Powered Muscle Stimulator, Transcutaneous Nerve |
| Stimulator, Interferential Current Stimulator, External | |
| Neuromuscular Functional Stimulator |
3. PREDICATE DEVICES
Empi Focus - K951951 JACE Tristim - K931871 RS Medical RS-4M+ - K000114
4. INTENDED USE
The 300 PV is a multifunction electrotherapy device with various treatment modes that allow for neuromuscular electrical stimulation (NMES), transcutaneous electrical nerve stimulation (TENS), interferential current stimulation (IFS) and functional electrical stimulation (FES).
1
KO 21100 2083
As a NMES device, the 300 PV is indicated for the following conditions:
- Retarding or preventing disuse atrophy .
- . Maintaining or increasing range of motion
- Re-educating muscles .
- Relaxation of muscle spasm .
- Increasing local blood circulation .
- Prevention of venous thrombosis of the calf muscles immediately after . surgery
As a TENS device, the 300 PV is indicated for the following conditions:
- Symptomatic relief and management of chronic, intractable pain .
- Adjunctive treatment for post-surgical and post-trauma acute pain .
As an IFS device, the 300 PV is indicated for the following conditions:
- Symptomatic relief of acute pain .
- Symptomatic relief and management of chronic pain .
As a FES device, the 300 PV is indicated for the following condition:
- Stimulation of the muscles in the leg and ankle of partially paralyzed . patients to provide flexion of the foot and thus improve the patient's gait.
DEVICE DESCRIPTION న.
The Empi 300 PV Complete Electrotherapy System (300 PV) is a battery-powered, multifunction device intended to provide clinicians with the flexibility to prescribe multiple stimulation therapy regimens with the same device. The 300 PV offers the following features:
- . Two independent stimulation channels (CH1 and CH2), each of which can provide NMES, TENS, IF, or FES therapy. HV therapy can be accomplished using CH1.
- Two independent intensity controls corresponding to each of the stimulation ● channels with a maximum stimulation of 100 mA from each channel.
- Timed therapy sessions
2
K021100
30F3
- Continuous or cycled stimulation
- . Adjustable pulse rates
- . Adjustable ON and OFF time controls
- . Balanced asymmetrical and symmetrical biphasic waveforms
- Thirteen preprogrammed regimens: five for NMES; one for TENS; one for ● IF; two for HV and four that can be customized by the clinician (two NMES and two HV).
- Lock option for clinician to control treatment regimens and stimulus intensity .
- Pause button for patient to pause stimulation. During pause, the timer will ● not countdown if timing has been set up. Upon restart, the device assumes the previous treatment stimulation parameters but a stimulus intensity of zero.
- . Optional external hand or foot switch used to control the device output during when used as an FES device for gait training
6. BASIS FOR SUBSTANTIAL EQUIVALENCE
The 300 PV is an extension of the Empi Focus and is similar in design and functions. Both offer preprogrammed treatment regimens, and the user can either choose one or more of these options or customize the treatment regimen within the available parameter ranges. The 300 PV incorporates several improvements over the Focus, including a simplified user interface for the preprogrammed regimens and the addition of the interferential and high voltage regimens. However, high voltage galvanic stimulation is available on the JACE Tristim and interferential current stimulation is available on the RS Medical RS-4M+.
3
Image /page/3/Picture/0 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circle with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" arranged around the circumference. Inside the circle is a stylized image of an eagle with three stripes representing its wings.
DEPARTMENT OF HEALTH & HUMAN SERVICES
Public Health Service
JUN 1 8 2002
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 .
Empi
C/O Sheila Hameon-Heyer, Esq., RAC Senior Staff Consultant Medical Device Consultants, Inc. 49 Plain Street North Attleboro, Massachusetts 02760
Re: K021100
Trade/Device Name: 300 PV Complete Electrotherapy System Regulation Number: 21 CFR 890.5850, 21 CFR 882.5810, 21 CFR 882.5890 and unclassified Regulation Name: Powered Electrical Muscle Stimulator, Functional Neuromuscular Electrical Stimulator, Transcutaneous Electrical Nerve Stimulator, and Interferential Current Electrical Stimulator Regulatory Class: Class II Product Code: IPF, GZI, GZJ and LIH Dated: April 2, 2002
Received: April 4, 2002
Dear Ms. Hameon-Heyer:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act
4
Page 2 - Ms. Hameon-Heyer, Esq., RAC
or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050,
This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and additionally 21 CFR Part 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4659. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html
Sincerely yours,
to Mark N Mellema
Celia M. Witten, Ph.D., M.D. Director Division of General, Restorative - and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
5
510(k) Number (if known):
Device Name: 300 PV COMPLETE ELECTROTHERAPY SYSTEM
Indications for Use:
The 300 PV is a multifunction electrotherapy device with various treatment modes that allow for neuromuscular electrical stimulation (NMES), transcutaneous electrical nerve stimulation (TENS), interferential current stimulation (IFS), and functional electrical stimulation (FES).
As a NMES device, the 300 PV is indicated for the following conditions:
- Retarding or preventing disuse atrophy .
- Maintaining or increasing range of motion ●
- Re-educating muscles ●
- Relaxation of muscle spasm .
- Increasing local blood circulation .
- Prevention of venous thrombosis of the calf muscles immediately after surgery .
As a TENS device, the 300 PV is indicated for the following conditions:
- Symptomatic relief and management of chronic, intractable pain .
- Adjunctive treatment for post-surgical and post-trauma acute pain .
As an IFS device, the 300 PV is indicated for the following conditions:
- Symptomatic relief of acute pain .
- Symptomatic relief and management of chronic pain .
As a FES device, the 300 PV is indicated for the following condition:
- Stimulation of the muscles in the leg and ankle of partially paralyzed patients to provide e flexion of the foot and thus improve the patient's gait.
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NECESSARY)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Mark N. Millken
Division Sign-Off) Division of General, Restorative and Neurological Devices
510(k) Number K021100
Prescription Use (Per 21 CFR 801.109) OR
Over-The-Counter Use
(Optional Format 1-2-96)
Empi 300 PV 510(k) April 2, 2002
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