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 oximeter
510(k) Number K071642
Device Name MEDIAID M960 SERIES, VITAL SIGNS MONITOR AND MEDIAID M900 SERIES, PULSE OXIMETER
Applicant
MEDIAID INC.
17517 FABRICA WAY, SUITE H
CERRITOS,  CA  90703
Applicant Contact JAYESH PATEL
Correspondent
MEDIAID INC.
17517 FABRICA WAY, SUITE H
CERRITOS,  CA  90703
Correspondent Contact JAYESH PATEL
Regulation Number870.2700
Classification Product Code
DQA  
Subsequent Product Code
DXN  
Date Received06/18/2007
Decision Date 05/02/2008
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-