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510(k) Data Aggregation
K Number
K003406Device Name
GUARDED NEEDLE 2000
Manufacturer
Date Cleared
2001-01-12
(72 days)
Product Code
Regulation Number
880.5570Why did this record match?
Applicant Name (Manufacturer) :
INTERNATIONAL MEDICAL DEVICE PARTNERS, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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