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 Holding Chambers, Direct Patient Interface
510(k) Number K070674
Device Name AEROCHAMBER PLUS ANTI-STATIC VALVED HOLDING CHAMBER WITH FLOW-VU INSPIRATORY FLOW INDICATOR
Applicant
Trudell Medical Intl.
725 Third St.
London,  CA N5V 5G4
Applicant Contact JOHN STRAATMAN
Correspondent
Trudell Medical Intl.
725 Third St.
London,  CA N5V 5G4
Correspondent Contact JOHN STRAATMAN
Regulation Number868.5630
Classification Product Code
NVP  
Date Received03/12/2007
Decision Date 04/11/2007
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Statement Statement
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-