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510(k) Data Aggregation

K Number

Device Name

MODIFICATION TO: PRONTO DRY

Manufacturer

MEDICAL INSTRUMENTS CORPORATION, AG

Date Cleared

2000-09-29

(51 days)

Product Code

Regulation Number

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Applicant Name (Manufacturer) :

MEDICAL INSTRUMENTS CORPORATION, AG

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

Device Description

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