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 Ventilator, Continuous, Facility Use
510(k) Number K040221
Device Name SERVO-I VENTILATOR SYSTEM, MODEL 64 87 800 E407E
Applicant
MAQUET CRITICAL CARE AB
186 WOOD AVENUE SOUTH
ISELIN,  NJ  08830
Applicant Contact JAMIE YIEH
Correspondent
MAQUET CRITICAL CARE AB
186 WOOD AVENUE SOUTH
ISELIN,  NJ  08830
Correspondent Contact JAMIE YIEH
Regulation Number868.5895
Classification Product Code
CBK  
Date Received02/02/2004
Decision Date 02/20/2004
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-