• 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 System, Environmental Control, Powered
510(k) Number K850314
Device Name TELEVISION CONTROL OPTION 1220
Applicant
Rehab Technology, Inc.
Box 185
Aviston,  IL  62216
Applicant Contact GEORGE ZURLIENE
Correspondent
Rehab Technology, Inc.
Box 185
Aviston,  IL  62216
Correspondent Contact GEORGE ZURLIENE
Regulation Number890.3725
Classification Product Code
IQA  
Date Received01/25/1985
Decision Date 04/25/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-