• 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 Transmitters And Receivers, Physiological Signal, Radiofrequency
510(k) Number K022274
Device Name CARECOMPANION PATIENT STATION & NURSE STATION
Applicant
Neptec Design Group, Ltd.
302 Legget Dr.
Kanata, Ontario,  CA K2K 1Y5
Applicant Contact JOHN SCHNEIDER
Correspondent
Neptec Design Group, Ltd.
302 Legget Dr.
Kanata, Ontario,  CA K2K 1Y5
Correspondent Contact JOHN SCHNEIDER
Regulation Number870.2910
Classification Product Code
DRG  
Date Received07/15/2002
Decision Date 05/29/2003
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-