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 Electrode, Depth
510(k) Number K902976
Device Name MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC
Applicant
MEDICAL CONSULTANTS INTL. LTD.
59 OXFORD PLACE
GLEN ROCK,  NJ  07452
Applicant Contact SAUL LISS
Correspondent
MEDICAL CONSULTANTS INTL. LTD.
59 OXFORD PLACE
GLEN ROCK,  NJ  07452
Correspondent Contact SAUL LISS
Regulation Number882.1330
Classification Product Code
GZL  
Date Received07/06/1990
Decision Date 09/07/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-