Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 Toothbrush, Powered
510(k) Number K860264
Device Name SCHERER PORTABLE TOOTH POLISHER
Applicant
Scherer Laboratories, Inc.
Arent,Fox,Kintner,Plotkin,Kahn
1050 Connecticut Ave., Nw.
Washington,  DC  20036
Applicant Contact W. R PENDERGAST
Correspondent
Scherer Laboratories, Inc.
Arent,Fox,Kintner,Plotkin,Kahn
1050 Connecticut Ave., Nw.
Washington,  DC  20036
Correspondent Contact W. R PENDERGAST
Regulation Number872.6865
Classification Product Code
JEQ  
Date Received01/27/1986
Decision Date 06/26/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-