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510(k) Data Aggregation

K Number

Device Name

NCI SPATULA

Manufacturer

FISCHER SURGICAL INC.

Date Cleared

2012-05-31

(442 days)

Product Code

Regulation Number

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Applicant Name (Manufacturer) :

FISCHER SURGICAL INC.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

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