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 plethysmograph, air displacement for body composition analysis
510(k) Number K060848
Device Name BOD POD
Applicant
LIFE MEASUREMENT, INC.
1850 BATES AVE.
CONCORD,  CA  94520 -8586
Applicant Contact MICHAEL SULLIVAN
Correspondent
LIFE MEASUREMENT, INC.
1850 BATES AVE.
CONCORD,  CA  94520 -8586
Correspondent Contact MICHAEL SULLIVAN
Regulation Number870.2770
Classification Product Code
OAC  
Date Received03/28/2006
Decision Date 06/27/2006
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Obstetrics/Gynecology
Summary Summary
Type Abbreviated
Reviewed by Third Party No
Combination Product No
-
-