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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 K883819
Device Name BULLARD INTUBATING LARYNGOSCOPE LAR-A & LAR-P
Applicant
Circon Acmi
300 Stillwater Ave.
P.O. Box 1971
Stamford,  CT  06904
Applicant Contact TAYLOR, PE
Correspondent
Circon Acmi
300 Stillwater Ave.
P.O. Box 1971
Stamford,  CT  06904
Correspondent Contact TAYLOR, PE
Regulation Number868.5540
Classification Product Code
CCW  
Date Received09/08/1988
Decision Date 10/17/1988
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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