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U.S. Department of Health and Human Services

510(K) Premarket Notification
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Device Name
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510(K)
Number
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Decision
Date
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rmi vascular tourniquet kit Research Medical, Inc. k910221 05/16/1991
barrier* extra protection plus face mask Johnson & Johnson Medical, Inc. k910557 04/29/1991
vpw 2877e6 x-ray power supply Varian Canada, Inc. k910820 03/07/1991
hewlett-packard models m1400a, m1402a & m1401a Hewlett-Packard Co. k911139 06/11/1991
custom personal ear - cpe Qualitone k911497 04/19/1991
coil field extender Resonex, Inc. k911800 07/03/1991
model 704 Ivy Biomedical Systems, Inc. k912139 03/25/1992
multichannel recording system Bionique k912427 07/26/1991
esophageal stethoscope temperature probe Spacelabs, Inc. k912742 04/20/1992
wilde light curing composite restorative resins Wilde-USA, Inc. k913089 04/21/1992

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