• 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 ventilator, non-continuous (respirator)
510(k) Number K041828
Device Name APEX MEDICAL CPAP MODEL 9S-003
Applicant
APEX MEDICAL CORP.
NO. 9, MINSHENG STREET
TUCHENG CITY, TAIPEI COUNTY,  TW 236
Applicant Contact ALAN CHANG
Correspondent
APEX MEDICAL CORP.
NO. 9, MINSHENG STREET
TUCHENG CITY, TAIPEI COUNTY,  TW 236
Correspondent Contact ALAN CHANG
Regulation Number868.5905
Classification Product Code
BZD  
Date Received07/07/2004
Decision Date 07/30/2004
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Statement Statement
Type Special
Reviewed by Third Party No
Combination Product No
-
-