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 K092641
Device Name CHARMCARE TABLETOP PULSE OXIMETER
Applicant
Charmcare Co., Ltd.
325 N. Puente St., Unit B
Brea,  CA  92821
Applicant Contact JOYCE BANG
Correspondent
Charmcare Co., Ltd.
325 N. Puente St., Unit B
Brea,  CA  92821
Correspondent Contact JOYCE BANG
Regulation Number870.2700
Classification Product Code
DQA  
Date Received08/27/2009
Decision Date 10/21/2010
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-