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 Stimulator, Muscle, Diagnostic
510(k) Number K842805
Device Name IMPULS 3, IT SELECTOR
Applicant
Robert Bosch Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Robert Bosch Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number890.1850
Classification Product Code
ISB  
Date Received07/17/1984
Decision Date 08/01/1984
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
-
-