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 Strip, Temperature, Forehead, Liquid Crystal
510(k) Number K820426
Device Name TEMPERATURE TREND INDICATOR (TTI)
Applicant
MON-A-THERM, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
MON-A-THERM, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number880.2200
Classification Product Code
KPD  
Date Received02/16/1982
Decision Date 03/08/1982
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-