• 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, Physical Therapy, Multi Function
510(k) Number K862022
Device Name LIC-ORTHION MULTI-THERAPY TREATMENT TABLE
Applicant
Lic-Orthion
C/O Dickstein, Shapiro & Morin
2101 L St., NW
Washington,  DC  20037
Applicant Contact RODNEY R MUNSEY
Correspondent
Lic-Orthion
C/O Dickstein, Shapiro & Morin
2101 L St., NW
Washington,  DC  20037
Correspondent Contact RODNEY R MUNSEY
Regulation Number890.5880
Classification Product Code
JFB  
Date Received05/28/1986
Decision Date 06/19/1986
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
-
-