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 Dynamometer, Ac-Powered
510(k) Number K880464
Device Name DYNATRON II
Applicant
DYNATRONICS LASER CORP.
470 LAWNDALE DRIVE, BUILDING
D
SALT LAKE CITY,  UT  84115
Applicant Contact STEVEN R WOODHEAD
Correspondent
DYNATRONICS LASER CORP.
470 LAWNDALE DRIVE, BUILDING
D
SALT LAKE CITY,  UT  84115
Correspondent Contact STEVEN R WOODHEAD
Regulation Number888.1240
Classification Product Code
LBB  
Date Received02/03/1988
Decision Date 03/08/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-