• 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 Airbrush
510(k) Number K955050
Device Name JETSTREAM CAVITY PREPARATION SYSTEM
Applicant
DOVE SYSTEMS, INC.
1000 BURNETT AVE.
SUITE 450
CONCORD,  CA  94520
Applicant Contact DAVID W SCHLERF
Correspondent
DOVE SYSTEMS, INC.
1000 BURNETT AVE.
SUITE 450
CONCORD,  CA  94520
Correspondent Contact DAVID W SCHLERF
Regulation Number872.6080
Classification Product Code
KOJ  
Date Received11/03/1995
Decision Date 03/07/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-