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510(k) Data Aggregation

K Number

Device Name

STAPLE REMOVAL KIT

Manufacturer

CONTINENTAL MEDICAL LABORATORIES, INC.

Date Cleared

1996-10-21

(63 days)

Product Code

Regulation Number

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Product Code :

GDT

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

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