LUXAR MODEL LX-20 CO2 LASER

FDA 510(k) Premarket Notification · Submission K904068 · Applicant: Luxar Corp.

Public Record 510(k) Submission Decision Date: 1991-04-15 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K904068.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K904068
Applicant / Sponsor
Device Name
LUXAR MODEL LX-20 CO2 LASER
Product Code
GEX
Decision Date
1991-04-15
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
General, Plastic Surgery (SU)
Clearance Type
Traditional
Third Party Flag
N
Date Received
1990-08-31

Related Establishments / Registrations

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