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510(k) Data Aggregation
K Number
K001295Device Name
PIPER
Manufacturer
RTEK MEDICAL SYSTEMS, LLC.
Date Cleared
2000-10-25
(184 days)
Product Code
MUJ
Regulation Number
892.5050Why did this record match?
Applicant Name (Manufacturer) :
RTEK MEDICAL SYSTEMS, LLC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
Device Description
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