• 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 interferential current therapy
510(k) Number K930264
Device Name MATRIX ELECDT & VACUPULLS
Applicant
MATRIX ELECTROMEDICAL, INC.
9545 BONITA VISTA ST.
LAS VEGAS,  NV  89131
Applicant Contact DEBORAH SORGNARD
Correspondent
MATRIX ELECTROMEDICAL, INC.
9545 BONITA VISTA ST.
LAS VEGAS,  NV  89131
Correspondent Contact DEBORAH SORGNARD
Regulation Number882.5890
Classification Product Code
LIH  
Date Received01/19/1993
Decision Date 06/29/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-