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510(k) Data Aggregation

K Number

Device Name

LARKEL DEVICE WITH ATTACHMENTS A-H(MODIFICATION)

Manufacturer

SEIDEL MEDIZIN GMBH

Date Cleared

1996-05-16

(331 days)

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Regulation Number

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Applicant Name (Manufacturer) :

SEIDEL MEDIZIN GMBH

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

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