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510(k) Data Aggregation
K Number
K962243Device Name
VASOTHERM
Manufacturer
Date Cleared
1997-02-21
(255 days)
Product Code
Regulation Number
890.5290Why did this record match?
Applicant Name (Manufacturer) :
EHTI MEDICAL CORP.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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K Number
K962703Device Name
THEE THERMASTIM
Manufacturer
Date Cleared
1997-02-21
(224 days)
Product Code
Regulation Number
890.5290Why did this record match?
Applicant Name (Manufacturer) :
EHTI MEDICAL CORP.
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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