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Found 5 results
510(k) Data Aggregation
K Number
K003010Device Name
SPIRIT ACUPUNCTURE NEEDLE
Manufacturer
UNITED PACIFIC CO., LTD.
Date Cleared
2000-10-19
(23 days)
Product Code
MQX
Regulation Number
880.5580Why did this record match?
Applicant Name (Manufacturer) :
UNITED PACIFIC CO., LTD.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
Device Description
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K Number
K001718Device Name
MILLENNIA ACUPUNCTURE NEEDLE
Manufacturer
UNITED PACIFIC CO., LTD.
Date Cleared
2000-06-21
(16 days)
Product Code
MQX
Regulation Number
880.5580Why did this record match?
Applicant Name (Manufacturer) :
UNITED PACIFIC CO., LTD.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
Device Description
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K Number
K993123Device Name
QK-WIDE BAND SPECTRUM THERAPEUTIC APPARATUS, MODELS CO1A, CO1B, CO1C, CO1D, CO2A, CO2B
Manufacturer
UNITED PACIFIC CO., LTD.
Date Cleared
1999-12-17
(88 days)
Product Code
ILY
Regulation Number
890.5500Why did this record match?
Applicant Name (Manufacturer) :
UNITED PACIFIC CO., LTD.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
Intented to use to emit energy in the infrared spectrum to provide topical heating for the purpose of temporarily elevating local tissue temperature.
Intended to use for the temporary relief of minor muscle and joint stiffness, temporary relief of minor muscle strain spasm, temporary increase in local circulation where applied, and the relaxation of muscle.
Device Description
Not Found
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K Number
K991503Device Name
SACRED CRANE TDP LAMP, MODELS CQ-27, CQ-12, CQ-36
Manufacturer
UNITED PACIFIC CO., LTD.
Date Cleared
1999-07-28
(90 days)
Product Code
ILY
Regulation Number
890.5500Why did this record match?
Applicant Name (Manufacturer) :
UNITED PACIFIC CO., LTD.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
To emit energy in the infrared spectrum to provide topical temperature. Intended to use for the temporary relief of minor muscle and joint stiffness, temporary increase in local circulation where applied, and the relaxation of muscles.
Device Description
Not Found
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K Number
K990406Device Name
KINGLI ACUPUNCTURE NEEDLE
Manufacturer
UNITED PACIFIC CO., LTD.
Date Cleared
1999-04-16
(66 days)
Product Code
MQX, MOX
Regulation Number
880.5580Why did this record match?
Applicant Name (Manufacturer) :
UNITED PACIFIC CO., LTD.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
to pierce the skin in the practice of acupuncture by the states.
Device Description
DISPOSABLE ACUPUNCTURE NEEDLE
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