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Found 8 results
510(k) Data Aggregation
K Number
K252218Device Name
MF SC GEN2 Facial Toning System
Manufacturer
Micro Current Technology, Inc.
Date Cleared
2025-07-18
(3 days)
Product Code
NFO
Regulation Number
882.5890Why did this record match?
Applicant Name (Manufacturer) :
Micro Current Technology, Inc.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
Device Description
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K Number
K233095Device Name
S21 OTC Transcutaneous Electrical Nerve Stimulator
Manufacturer
Micro Current Technology, Inc.
Date Cleared
2024-03-01
(157 days)
Product Code
NUH
Regulation Number
882.5890Why did this record match?
Applicant Name (Manufacturer) :
Micro Current Technology, Inc.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
Intended for the symptomatic relief and management of chronic intractable pain, and as an adjunctive treatment for postsurgical and post-trauma acute pain. The device is indicated for over the counter use.
Device Description
Not Found
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K Number
K233525Device Name
MF SC Facial Toning System
Manufacturer
Micro Current Technology, Inc.
Date Cleared
2023-11-24
(23 days)
Product Code
NFO
Regulation Number
882.5890Why did this record match?
Applicant Name (Manufacturer) :
Micro Current Technology, Inc.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The MF SC Facial Toning System is intended to stimulate the face. The device is indicated for over the counter cosmetic use.
Device Description
Not Found
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K Number
K183189Device Name
Ultra OTC Facial Toning System
Manufacturer
Micro Current Technology, Inc.
Date Cleared
2019-04-17
(149 days)
Product Code
NFO
Regulation Number
882.5890Why did this record match?
Applicant Name (Manufacturer) :
Micro Current Technology, Inc.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
Not Found
Device Description
Not Found
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K Number
K181062Device Name
Ultra Facial Toning System
Manufacturer
Micro Current Technology, Inc.
Date Cleared
2018-07-18
(86 days)
Product Code
NFO
Regulation Number
882.5890Why did this record match?
Applicant Name (Manufacturer) :
Micro Current Technology, Inc.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The Ultra Facial Toning System is intended to stimulate the face. The device is intended for cosmetic use.
Device Description
Not Found
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K Number
K033253Device Name
S21 TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR
Manufacturer
MICRO CURRENT TECHNOLOGY, INC.
Date Cleared
2003-10-21
(13 days)
Product Code
GZJ
Regulation Number
882.5890Why did this record match?
Applicant Name (Manufacturer) :
MICRO CURRENT TECHNOLOGY, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The S21 Transcutaneous Electrical Nerve Stimulator (TENS) device is intended to by used by physicians or licensed practitioners for symptomatic relief of chronic intractable pain by sending electrical impulses through the skin to the nerves lying directly beneath the skin surface. These impulses help to block the body's ability to send a pain message to the brain, thereby reducing the pain sensation. The S21 is a dual channel device that produces constant micro ampere currents with the selected envelopes, waveforms, frequencies, and polarity, with a maximum voltage of 30 volts.
Device Description
The S21 is a dual channel device that produces constant micro ampere currents with the selected envelopes, waveforms, frequencies, and polarity, with a maximum voltage of 30 volts.
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K Number
K032653Device Name
E275
Manufacturer
MICRO CURRENT TECHNOLOGY, INC.
Date Cleared
2003-09-12
(15 days)
Product Code
GZJ
Regulation Number
882.5890Why did this record match?
Applicant Name (Manufacturer) :
MICRO CURRENT TECHNOLOGY, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The E275 Transcutaneous Electrical Nerve Stimulator (TENS) device is intended to by used by physicians or licensed practitioners for symptomatic relief of chronic intractable pain by sending electrical impulses through the skin to the nerves lying directly beneath the skin surface. These impulses help to block the body's ability to send a pain message to the brain, thereby reducing the pain sensation.
Device Description
The E275 is a dual channel device that produces constant micro ampere currents with the selected envelopes, waveforms; frequencies, and polarity, with a maximum voltage of 30 volts.
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K Number
K993823Device Name
MED-4000
Manufacturer
MICRO CURRENT TECHNOLOGY, INC.
Date Cleared
1999-11-19
(7 days)
Product Code
GZJ, DAT
Regulation Number
882.5890Why did this record match?
Applicant Name (Manufacturer) :
MICRO CURRENT TECHNOLOGY, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The MED 4000 Transcutaneous Electrical Nerve Stimulator (TENS) device is intended to by used by physicians or licensed practitioners for symptomatic relief of chronic intractable pain by sending electrical impulses through the skin to the nerves lying directly beneath the skin suarane impulses help to block the body's ability to send a pain message to the brain, thereby reducing the pair. sensation.
Device Description
The MED 4000 is a dual channel device that produces constant micro ampere currents with the selected envelopes, waveforms, frequencies, and polarity, with a maximum voltage of 30 volts.
Ask a Question
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