• 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 Continuous Measurement Thermometer
510(k) Number K851873
Device Name FORTEC MI-305
Applicant
Nam Tai , Ltd.
12/F. & 13/F., Century Centre
44-46 Hungt To Rd. Kwun Tong
Kowloon, Hong Kong,  HK
Applicant Contact WILSON WANG
Correspondent
Nam Tai , Ltd.
12/F. & 13/F., Century Centre
44-46 Hungt To Rd. Kwun Tong
Kowloon, Hong Kong,  HK
Correspondent Contact WILSON WANG
Regulation Number880.2910
Classification Product Code
FLL  
Date Received04/29/1985
Decision Date 05/13/1985
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
-
-