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 Transport, Patient, Powered
510(k) Number K890555
Device Name PATIENT MOVER(TM)
Applicant
T.B.S., Inc.
2894 Bunsen Ave., Unit J
Ventura,  CA  93003
Applicant Contact BOB KNOUSE
Correspondent
T.B.S., Inc.
2894 Bunsen Ave., Unit J
Ventura,  CA  93003
Correspondent Contact BOB KNOUSE
Regulation Number890.5150
Classification Product Code
ILK  
Date Received02/06/1989
Decision Date 02/13/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-