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510(k) Data Aggregation

K Number

Device Name

CRANIOCAP

Manufacturer

GILLETTE CHILDREN'S SPECIALTY HEALTHCARE

Date Cleared

2000-10-30

(227 days)

Product Code

Regulation Number

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Applicant Name (Manufacturer) :

GILLETTE CHILDREN'S SPECIALTY HEALTHCARE

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

Device Description

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