• 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 Monitor, Airway Pressure (Includes Gauge And/Or Alarm)
510(k) Number K925673
Device Name AIRWAY PRESSURE MONITOR CM 5000 NGAN
Applicant
CANADIAN MONAGHAN LTD.
220 ADELAIDE ST. SOUTH
LONDON, ONTARIO,  CA N5Z 3L1
Applicant Contact CAROL MASON
Correspondent
CANADIAN MONAGHAN LTD.
220 ADELAIDE ST. SOUTH
LONDON, ONTARIO,  CA N5Z 3L1
Correspondent Contact CAROL MASON
Regulation Number868.2600
Classification Product Code
CAP  
Date Received11/10/1992
Decision Date 06/09/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-