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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia
510(k) Number K924679
Device Name OXYCARE(TM) OXYGEN CONTROLLER/MONITOR
Applicant
AIR-SHIELDS VICKERS, INC.
330 JACKSONVILLE RD.
HATBORO,  PA  19040
Applicant Contact FRANCIS X CASEY
Correspondent
AIR-SHIELDS VICKERS, INC.
330 JACKSONVILLE RD.
HATBORO,  PA  19040
Correspondent Contact FRANCIS X CASEY
Regulation Number868.2500
Classification Product Code
KLK  
Date Received09/16/1992
Decision Date 02/21/1995
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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