KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+


Device Classification Name

laser, dental, soft tissue

510(k) Number K030146
Device Name KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+
Original Applicant
KAVO AMERICA
340 east main st.
lake zurich, 
IL 
60047

Original Contact j0hn r franz
Regulation Number 878.4810
Classification Product Code
NVK  
Date Received 01/15/2003
Decision Date 08/03/2005
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No