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510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

MRI'S ALL SILICONE FOLEY CATHETER

Manufacturer

MRI MANUFACTURING AND RESEARCH, INC.

Date Cleared

1996-04-05

(561 days)

Product Code

Regulation Number

Type

Panel

Gastroenterology/Urology

Age Range

N/A

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N/A

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N/A

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

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