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, emergency, powered (resuscitator)
510(k) Number K910699
Device Name LIFE-02 (NON-REFILLABLE CYLINDER)
Applicant
LIFE CORP.
P.O. BOX 300
W140 N5566 LILLY ROAD
MENOMONEE FALLS,  WI  53051
Applicant Contact JOHN KIRCHGERORG
Correspondent
LIFE CORP.
P.O. BOX 300
W140 N5566 LILLY ROAD
MENOMONEE FALLS,  WI  53051
Correspondent Contact JOHN KIRCHGERORG
Regulation Number868.5925
Classification Product Code
BTL  
Date Received02/19/1991
Decision Date 06/18/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-