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Found 2 results

510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

DORNIER MEDILAS D SKINPULSE LASER SYSTEM (SKINPULSE)

Manufacturer

DORNIER SURGICAL PRODUCTS, INC.

Date Cleared

2001-03-26

(90 days)

Product Code

Regulation Number

Type

Panel

General & Plastic Surgery

Age Range

N/A

Reference & Predicate Devices

N/A

Predicate For

K020339,K024064,K041930,K053540,K070536,K073427

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

Ask a Question

Ask a specific question about this device

K Number

Validate with FDA (Live)

Device Name

DORNIER MEDILAS D SKINPULSE

Manufacturer

DORNIER SURGICAL PRODUCTS, INC.

Date Cleared

2000-06-12

(154 days)

Product Code

Regulation Number

Type

Panel

General & Plastic Surgery

Age Range

N/A

Reference & Predicate Devices

N/A

Predicate For

K020339,K053540,K070536,K073427

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

Ask a Question

Ask a specific question about this device

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