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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name circuit, breathing (w connector, adaptor, y piece)
510(k) Number K945984
Device Name MERIDIAN MEDICAL SYSTEMS MAPLESON D AND MODIFIED JACKSON REESE CIRCUITS
Applicant
MERIDIAN MEDICAL SYSTEMS, INC.
8102 WOOD LAND DR.
INDIANAPOLIS,  IN  46278
Applicant Contact ROBERT RICHMOND
Correspondent
MERIDIAN MEDICAL SYSTEMS, INC.
8102 WOOD LAND DR.
INDIANAPOLIS,  IN  46278
Correspondent Contact ROBERT RICHMOND
Regulation Number868.5240
Classification Product Code
CAI  
Date Received12/08/1994
Decision Date 12/27/1994
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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