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 laryngoscope, rigid
510(k) Number K861026
Device Name LIBAN INTUBATOR
Applicant
LIFE SUPPORT DEVICES CO.
C/O STEFAN LIBAN
13911 OLD HARBOR LANE, STE 304
MARINA DEL REY,  CA  90291
Applicant Contact RICHARD CARSTENS
Correspondent
LIFE SUPPORT DEVICES CO.
C/O STEFAN LIBAN
13911 OLD HARBOR LANE, STE 304
MARINA DEL REY,  CA  90291
Correspondent Contact RICHARD CARSTENS
Regulation Number868.5540
Classification Product Code
CCW  
Date Received03/18/1986
Decision Date 07/28/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-