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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name connector, airway (extension)
510(k) Number K894969
Device Name AEROVENT
Applicant
MONAGHAN MEDICAL CORP.
FRANKLYN BLDG RT. 9 NORTH
P.O. BOX 978
PLATTSBURGH,  NY  12901
Applicant Contact JAMES A COCHIE
Correspondent
MONAGHAN MEDICAL CORP.
FRANKLYN BLDG RT. 9 NORTH
P.O. BOX 978
PLATTSBURGH,  NY  12901
Correspondent Contact JAMES A COCHIE
Regulation Number868.5810
Classification Product Code
BZA  
Date Received08/07/1989
Decision Date 10/30/1989
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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