• 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 chair, dental, with operative unit
510(k) Number K760322
Device Name CHAIR, ATTACHED INSTRUMENT DEL. SYS.
Applicant
THE S. S. WHITE CO.
803 N. Front St. Suite 3
mchenry,  IL  60050
Correspondent
THE S. S. WHITE CO.
803 N. Front St. Suite 3
mchenry,  IL  60050
Regulation Number872.6250
Classification Product Code
KLC  
Date Received07/26/1976
Decision Date 08/03/1976
Decision substantially equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-