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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 K954787
Device Name ILLUMINATOR
Applicant
HOSPITAK, INC.
10 DANIEL ST.
FARMINGDALE,  NY  11735
Applicant Contact WILLIAM LACCY
Correspondent
HOSPITAK, INC.
10 DANIEL ST.
FARMINGDALE,  NY  11735
Correspondent Contact WILLIAM LACCY
Regulation Number868.5540
Classification Product Code
CCW  
Date Received10/18/1995
Decision Date 01/31/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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