• 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 Table, Radiographic, Non-Tilting, Powered
510(k) Number K771601
Device Name X-RAY REMOTE CONTROL TABLE
Applicant
Toshiba Medical Systems
4221 Richmond Rd., NW
Walker,  MI  49534
Correspondent
Toshiba Medical Systems
4221 Richmond Rd., NW
Walker,  MI  49534
Regulation Number892.1980
Classification Product Code
IZZ  
Date Received08/19/1977
Decision Date 09/20/1977
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-