• 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 K883437
Device Name DENTAL CHAIR
Applicant
E.F. Brewer Co.
13901 Main St.
P.O. Box 159
Menomonee Falls,  WI  53051
Applicant Contact DON HOULBERG
Correspondent
E.F. Brewer Co.
13901 Main St.
P.O. Box 159
Menomonee Falls,  WI  53051
Correspondent Contact DON HOULBERG
Regulation Number872.6250
Classification Product Code
KLC  
Date Received08/15/1988
Decision Date 10/12/1988
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
-
-