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510(k) Data Aggregation
K Number
K000135Device Name
PRO.DUCT CATHETER, MODEL CTH03
Manufacturer
Date Cleared
2000-04-10
(83 days)
Product Code
Regulation Number
876.1075Why did this record match?
Applicant Name (Manufacturer) :
PRO.DUCT HEALTH, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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