Picosure Workstation

FDA 510(k) Premarket Notification · Submission K143105 · Applicant: Cynosure, Inc.

Public Record 510(k) Submission Decision Date: 2015-02-23 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K143105.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K143105
Applicant / Sponsor
Device Name
Picosure Workstation
Product Code
GEX
Decision Date
2015-02-23
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
General, Plastic Surgery (SU)
Clearance Type
Traditional
Third Party Flag
N
Date Received
2014-10-29

Related Establishments / Registrations

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