DIOLASE 980 D LASER SYSTEM

FDA 510(k) Premarket Notification · Submission K023547 · Applicant: American Dental Technologies, Inc.

Public Record 510(k) Submission Decision Date: 2003-04-15 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K023547.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K023547
Device Name
DIOLASE 980 D LASER SYSTEM
Product Code
GEX
Decision Date
2003-04-15
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
General, Plastic Surgery (SU)
Clearance Type
Traditional
Third Party Flag
N
Date Received
2002-10-21

Related Establishments / Registrations

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