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 thermometer, electronic, clinical
510(k) Number K905025
Device Name DIGITAL THERMOMETER KITS
Applicant
ABCO DEALERS, INC.
6601 W. MILL RD.
P.O. BOX 23090
MILWAUKEE,  WI  53218 -1238
Applicant Contact MOLLY PETR
Correspondent
ABCO DEALERS, INC.
6601 W. MILL RD.
P.O. BOX 23090
MILWAUKEE,  WI  53218 -1238
Correspondent Contact MOLLY PETR
Regulation Number880.2910
Classification Product Code
FLL  
Date Received11/07/1990
Decision Date 02/07/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-