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 System, Isokinetic Testing And Evaluation
510(k) Number K904898
Device Name TORQUE FRAME QTF1000
Applicant
Medmetric Corp.
7542 Trade St.
San Diego,  CA  92121
Applicant Contact WATKINS
Correspondent
Medmetric Corp.
7542 Trade St.
San Diego,  CA  92121
Correspondent Contact WATKINS
Regulation Number890.1925
Classification Product Code
IKK  
Date Received10/30/1990
Decision Date 11/28/1990
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
-
-