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, Nerve, Transcutaneous, For Pain Relief
510(k) Number K954334
Device Name ACUPLUS
Applicant
S.H.P. INTL. PTY., LTD.
2322 DOUGLAS DR.
EUGENE,  OR  97405 -1711
Applicant Contact ROBERT S MCQUATE
Correspondent
S.H.P. INTL. PTY., LTD.
2322 DOUGLAS DR.
EUGENE,  OR  97405 -1711
Correspondent Contact ROBERT S MCQUATE
Regulation Number882.5890
Classification Product Code
GZJ  
Date Received09/18/1995
Decision Date 01/22/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-