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510(k) Data Aggregation

K Number

Device Name

MICRODOSE CATH, MODELS 90121-201, -202, -203

Manufacturer

Date Cleared

2001-06-25

(49 days)

Product Code

Regulation Number

Why did this record match?

Applicant Name (Manufacturer) :

DURECT CORP.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

Device Description

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