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510(k) Data Aggregation

K Number

Device Name

LOKKI DT

Manufacturer

HILLARD W. WELCH

Date Cleared

1999-03-15

(376 days)

Product Code

Regulation Number

Why did this record match?

Applicant Name (Manufacturer) :

HILLARD W. WELCH

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

Pulpotomy Filling material such as gutta percha or resin bakelite removal as adjunct treatment during root canal retreatment

Device Description

Not Found

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