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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 K930804
Device Name FILLISCOPE
Applicant
FILLISCOPE, INC.
950 LOUISIANA SE
ALBUQUERQUE,  NM  87108
Applicant Contact MESOUD FILLI
Correspondent
FILLISCOPE, INC.
950 LOUISIANA SE
ALBUQUERQUE,  NM  87108
Correspondent Contact MESOUD FILLI
Regulation Number868.5540
Classification Product Code
CCW  
Date Received02/16/1993
Decision Date 10/07/1993
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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