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510(k) Data Aggregation
(259 days)
SYS*STIM 240
- Indications for Medium Frequency (Russian), Biphasic, High Volt Pulsed Current (HVPC), Interferential (4P) and Premodulated (2P) waveforms
- Relaxation of muscle spasms
- Prevention or retardation of disuse atrophy
- Increase local blood circulation
- Muscle re-education
- Maintaining or increasing range of motion
- Immediate post-surgical stimulation of calf muscles to prevent venous thrombosis
- Additional indications for Microcurrent, Interferential (4P), Premodulated (2P), Biphasic and TENS waveforms
- Symptomatic relief and management of chronic, intractable pain
- Post-traumatic acute pain
- Post-surgical acute pain
- Indications for DC (Direct Current) Mode
- Relaxation of muscle spasm
- The laser and cluster applicators of the Sys*Stim 240 emit infrared energy for:
- Temporary increase in local blood circulation
- Temporary relief of minor muscle and joint aches, pains and stiffness
- Relaxation of muscles
- Temporary relief of muscle spasms
- Temporary relief of minor pain and stiffness associated with arthritis
The new Sys*Stim® 240 neuromuscular stimulator features nine discrete waveforms designed to facilitate clinical versatility. Waveforms may be combined with on-off programs for neuromuscular education as well as frequency and amplitude modulation programs for optimal pain management.
New touch-sensitive technology has been used to make starting a treatment easy. The high-resolution color display allows clinicians to monitor all treatment parameters continuously. The patented M Wheel™ provides easy navigation through all of the menus.
Clinicians can add full-featured light therapy capabilities to the SysStim 240 by purchasing either the cluster or laser applicator package. The laser applicator has an 80 mW, 785 nm, laser diode and the cluster emits 500 mW at 600 and 950 nm. Applicator holders are provided with each applicator and can be attached to the sides of the SysStim 240.
Treatment protocols complete with electrode placement quidance allow clinicians to quickly program treatment parameters for their patients. There is even space to save special treatment protocols for each waveform and for light therapy.
The Sys*Stim 240 has an optional battery pack so that clinicians can take either electrical stimulation or light therapy to their patients. A carrying case is also available which holds the units and all the accessories necessary for therapy on the road.
The Mettler Sys*Stim 240 is a neuromuscular stimulator and low-level light therapy device. The provided text describes its features, intended uses, and lists performance testing certifications but does not contain information about a study proving specific performance acceptance criteria for diagnostic or clinical efficacy aspects that would typically require a test set, ground truth, or expert evaluation.
Instead, the acceptance criteria and supporting "study" are focused on compliance with established electrical safety, electromagnetic compatibility (EMC), and laser safety standards, as well as showing substantial equivalence to a predicate device based on technical specifications and functional capabilities.
Here's a breakdown of the information requested, based on the provided text:
1. A table of acceptance criteria and the reported device performance
The acceptance criteria are primarily compliance with various electrical safety and performance standards. The "reported device performance" is the certification of compliance.
Acceptance Criteria (Standard Compliance) | Reported Device Performance (Certification) |
---|---|
ITS certification for ETL and C-ETL Listing | Certified |
Compliance with EMC, EN 60601-1-2: 2001 and FCC's 47 CFR, FCC Sub Part 18 | Certified |
Compliance to IEC 60601-2-22: 2007 | Certified |
Compliance to IEC 60825-1: 2007 | Certified |
Compliance to IEC 62471: 2006 | Certified |
Compliance to EN60601-2-10, (IEC 601-2-10) 2001 | Certified |
ISO 14971 : 2000 (Risk Management) | Yes (Claimed for comparison with predicate) |
UL 60601-1 (Medical Electrical Equipment) | Yes (Claimed for comparison with predicate) |
CSA C22.2 NO 601.1-M90 (Medical Electrical Equipment) | Yes (Claimed for comparison with predicate) |
IEC/EN 60601-1 (Medical Electrical Equipment) | Yes (Claimed for comparison with predicate) |
IEC/EN 60601-1-2 (EMC) | Yes (Claimed for comparison with predicate) |
IEC/EN 60601-2-10 (Nerve and muscle stimulators) | Yes (Claimed for comparison with predicate) |
MDD 93/42/EEC, Annex II (Medical Device Directive) | Yes (Claimed for comparison with predicate) |
Compliance with 21 CFR 898 (Performance Standards for Diagnostic X-Ray Systems) | Yes (Claimed for comparison with predicate) |
Patient Leakage Current (Normal Condition) |
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