• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name instrument, ultrasonic surgical
510(k) Number K993868
Device Name THE SOUNDVASER DISSECTION SYSTEM
Applicant
SOUND SURGICAL TECHNOLOGIES LLC.
1300 PLAZA CT. NORTH, #203
LAFAYETTE,  CO  80026
Applicant Contact WILLIAM W CIMINO
Correspondent
SOUND SURGICAL TECHNOLOGIES LLC.
1300 PLAZA CT. NORTH, #203
LAFAYETTE,  CO  80026
Correspondent Contact WILLIAM W CIMINO
Classification Product Code
LFL  
Date Received11/15/1999
Decision Date 12/21/1999
Decision Substantially Equivalent (SESE)
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-