• 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 Valve, Non-Rebreathing
510(k) Number K873570
Device Name LIFECARE EXHALATION VALVE #06-699
Applicant
LIFECARE SERVICES, INC.
655 ASPEN RIDGE DR.
LAFAYETTE,  CO  80026
Applicant Contact HAROLD ELLERINGTON
Correspondent
LIFECARE SERVICES, INC.
655 ASPEN RIDGE DR.
LAFAYETTE,  CO  80026
Correspondent Contact HAROLD ELLERINGTON
Regulation Number868.5870
Classification Product Code
CBP  
Date Received09/02/1987
Decision Date 11/30/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-