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510(k) Data Aggregation
K Number
K013585Device Name
MEDIPORT 2000 MOBILE
Manufacturer
Date Cleared
2002-01-28
(90 days)
Product Code
Regulation Number
878.4780Why did this record match?
Applicant Name (Manufacturer) :
SERVOX MEDIZINTECHNIK GMBH
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
The Mediport 2000 suction device can be generally used in the ENT sector and is equally suitable for both in-patient and outpatient purposes. It can be used for faryngectomy and in the event of heavy secretion in one of the organisms or other operations in the mouth and throut area. The mobile may only be used for the applications listed above.
Device Description
Mediport 2000 Mobile is a powered suction pump.
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