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 System, X-Ray, Fluoroscopic, Image-Intensified
510(k) Number K871743
Device Name VIDEO PLUS MODELS VP500, VP500A AND VP1000
Applicant
Camtronics, Ltd.
P.O. Box 307
Delafield,  WI  53018
Applicant Contact STEPHEN B SERVAIS
Correspondent
Camtronics, Ltd.
P.O. Box 307
Delafield,  WI  53018
Correspondent Contact STEPHEN B SERVAIS
Regulation Number892.1650
Classification Product Code
JAA  
Date Received05/05/1987
Decision Date 06/22/1987
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
-
-