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
510(k) Number K854194
Device Name IMT ULTRASONIC STRIDE MONITOR
Applicant
Innovative Medical Technologies, Inc.
2309 N. Commonwealth Ave.,
Suite 3w
Chicago,  IL  60614
Applicant Contact JOHN L TRIMBLE
Correspondent
Innovative Medical Technologies, Inc.
2309 N. Commonwealth Ave.,
Suite 3w
Chicago,  IL  60614
Correspondent Contact JOHN L TRIMBLE
Date Received10/15/1985
Decision Date 05/02/1986
Decision Substantially Equivalent (SESE)
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-