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
510(k) Number K863014
Device Name ISOPRAT F-III SET/ISOLAX CHAIR
Applicant
Sds Dental, Inc.
4321 Wisconsin Ave. N.W
Suite 200
Washington,  DC  20016
Applicant Contact CESAR CORAL
Correspondent
Sds Dental, Inc.
4321 Wisconsin Ave. N.W
Suite 200
Washington,  DC  20016
Correspondent Contact CESAR CORAL
Date Received08/08/1986
Decision Date 10/01/1986
Decision Substantially Equivalent (SESE)
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-