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, Powered
510(k) Number K900647
Device Name SOUTHERN CROSS HI-V4 PULSED HIGH VOLTAGE GALVANIC
Applicant
Nor-Am Patient Care Products, Inc.
P.O. Box 543
Lewiston,  NY  14092
Applicant Contact PAUL A JONES
Correspondent
Nor-Am Patient Care Products, Inc.
P.O. Box 543
Lewiston,  NY  14092
Correspondent Contact PAUL A JONES
Regulation Number890.5850
Classification Product Code
IPF  
Date Received02/09/1990
Decision Date 10/22/1990
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
-
-