• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Premarket Approval (PMA)

  • 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
Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
DeviceVH8500 HYPERTHERMIA TREATMENT SYSTEM
Classification Nameapplicator, hyperthermia, interstitial
Generic Nameapplicator, hyperthermia, interstitial
Applicant
COOK, INC.
p.o. box 489
bloomington, IN 47402
PMA NumberP880078
Supplement NumberS009
Date Received07/13/1992
Decision Date08/31/1992
Product Code
LMZ[ Registered Establishments with LMZ ]
Advisory Committee Radiology
Supplement Typenormal 180 day track
Supplement Reason change design/components/specifications/material
Expedited Review Granted? No
Combination Product No
-
-