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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 K880683
Device Name KING SYSTEMS, DISP. ANESTHESIA BREATHING CIRCUIT
Applicant
KING SYSTEMS CORP.
15011 HERRIMAN BLVD.
P.O. BOX 1138
NOBLESVILLE,  IN  46060
Applicant Contact LINDA L NORDLUND
Correspondent
KING SYSTEMS CORP.
15011 HERRIMAN BLVD.
P.O. BOX 1138
NOBLESVILLE,  IN  46060
Correspondent Contact LINDA L NORDLUND
Regulation Number868.5240
Classification Product Code
CAI  
Date Received02/19/1988
Decision Date 03/09/1988
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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