EVLT KIT AND THE D15PLUS AND D30PLUS DIODE LASERS

FDA 510(k) Premarket Notification · Submission K041957 · Applicant: Diomed, Inc.

Public Record 510(k) Submission Decision Date: 2004-12-01 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K041957.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K041957
Applicant / Sponsor
Device Name
EVLT KIT AND THE D15PLUS AND D30PLUS DIODE LASERS
Product Code
GEX
Decision Date
2004-12-01
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
General, Plastic Surgery (SU)
Clearance Type
Traditional
Third Party Flag
N
Date Received
2004-07-21

Related Establishments / Registrations

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