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510(k) Data Aggregation
K Number
K011518Device Name
VITALSAT SERIES
Manufacturer
Date Cleared
2002-11-15
(547 days)
Product Code
Regulation Number
870.2700Why did this record match?
Applicant Name (Manufacturer) :
BETA BIOMED SERVICES, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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K Number
K003542Device Name
PREAMP CABLE, MODEL B400-1011PA
Manufacturer
Date Cleared
2001-04-06
(140 days)
Product Code
Regulation Number
870.2700Why did this record match?
Applicant Name (Manufacturer) :
BETA BIOMED SERVICES, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
Ask a Question
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