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U.S. Department of Health and Human Services

510(k) Premarket Notification
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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 Ln., Suite 304
Marina Del Rey,  CA  90291
Applicant Contact RICHARD CARSTENS
Correspondent
Life Support Devices Co.
C/O Stefan Liban
13911 Old Harbor Ln., Suite 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
Predetermined Change
Control Plan Authorized		 No
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