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 Table, Mechanical
510(k) Number K892697
Device Name E653 OBLONG ABDUCTION BLOCK
Applicant
Rifton Equipment For the Handicapped
Rte. 213
Rifton,  NY  12471
Applicant Contact JOHN RHODES
Correspondent
Rifton Equipment For the Handicapped
Rte. 213
Rifton,  NY  12471
Correspondent Contact JOHN RHODES
Regulation Number890.3750
Classification Product Code
INW  
Date Received04/13/1989
Decision Date 05/09/1989
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
-
-