• 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 warmer, infant radiant
510(k) Number K122267
Device Name GIRAFFE AND PANDA WARMERS
Applicant
OHMEDA MEDICAL, A DIVISION OF DATEX-OHMEDA, INC.,
8880 GORMAN RD.
LAUREL,  MD  20723
Applicant Contact AGATA ANTHONY
Correspondent
OHMEDA MEDICAL, A DIVISION OF DATEX-OHMEDA, INC.,
8880 GORMAN RD.
LAUREL,  MD  20723
Correspondent Contact AGATA ANTHONY
Regulation Number880.5130
Classification Product Code
FMT  
Date Received07/30/2012
Decision Date 10/02/2012
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-