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510(k) Data Aggregation
K Number
K961217Device Name
BODILY FLUID DISPOSAL KIT
Manufacturer
Date Cleared
1996-07-25
(119 days)
Product Code
Regulation Number
878.4040Why did this record match?
Applicant Name (Manufacturer) :
TRANSIDYNE GENERAL CORP.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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K Number
K955658Device Name
LACERATION TRAY
Manufacturer
Date Cleared
1996-01-25
(44 days)
Product Code
Regulation Number
880.6850Why did this record match?
Applicant Name (Manufacturer) :
TRANSIDYNE GENERAL CORP.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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