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510(k) Data Aggregation
K Number
K003842Device Name
PRESCOTT'S SURGICAL SPEARManufacturer
Date Cleared
2001-04-13
(122 days)
Product Code
Regulation Number
886.4790Type
TraditionalPanel
OphthalmicReference & Predicate Devices
N/A
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Applicant Name (Manufacturer) :
PRESCOTT'S, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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