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510(k) Data Aggregation
K Number
K962837Device Name
NULIFE
Manufacturer
Date Cleared
1996-10-02
(85 days)
Product Code
Regulation Number
878.4460Why did this record match?
Applicant Name (Manufacturer) :
**MED-TECH RUBBER **& ENGINEERING INDUSTRIES
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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K Number
K955055Device Name
NULIFE
Manufacturer
Date Cleared
1996-01-23
(81 days)
Product Code
Regulation Number
880.6250Why did this record match?
Applicant Name (Manufacturer) :
**MED-TECH RUBBER **& ENGINEERING INDUSTRIES
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
Ask a Question
Ask a specific question about this device
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