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510(k) Data Aggregation
K Number
K955474Device Name
NEO-PNEUMOCATH
Manufacturer
Date Cleared
1996-02-13
(75 days)
Product Code
Regulation Number
878.4200Why did this record match?
Applicant Name (Manufacturer) :
INTRA SPECIAL CATHETERS GMBH
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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