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 Device, Galvanic Skin Response Measurement
510(k) Number K883112
Device Name DERMATRON SKIN RESISTANCE METER
Applicant
RAYMAR ELECTRONICS
P.O. BOX 16, FAIRVIEW ESTATE
READING ROAD,HENLEY-ON-THAMES
OXON RG9 1LL, ENGLAND,  GB
Applicant Contact RAYMOND HODGKINSON
Correspondent
RAYMAR ELECTRONICS
P.O. BOX 16, FAIRVIEW ESTATE
READING ROAD,HENLEY-ON-THAMES
OXON RG9 1LL, ENGLAND,  GB
Correspondent Contact RAYMOND HODGKINSON
Regulation Number882.1540
Classification Product Code
GZO  
Date Received07/25/1988
Decision Date 08/10/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-