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510(k) Data Aggregation

K Number

Device Name

AMS FASCIAL-ANCHORING SYSTEM

Manufacturer

AMERICAN MEDICAL SYSTEMS, INC.

Date Cleared

2001-03-26

(55 days)

Product Code

Regulation Number

Why did this record match?

Product Code :

NEH

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

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