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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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arthro-prep rest NORTHWEST SURGICAL CONCEPTS, INC. k812396 11/20/1981
lateral angulating fluoro suspension sys GENERAL ELECTRIC CO. k812561 10/13/1981
adaptaid #365-38 INTERMEDICS, INC. k812756 10/29/1981
lancer specimen container SHERWOOD MEDICAL CO. k812933 11/06/1981
atrial endocardial electrode lead j-tip TELECTRONICS, INC. k813134 12/10/1981
trocki body ventrilator L.T.D. 3 CO. k813326 12/22/1981
oms infusion-aspiration handle OPTICAL MICRO SYSTEMS, INC. k813500 02/04/1982
anesthesiology devices BENTLEY LABORATORIES, INC. k820046 01/29/1982
norton flow directed thermodilution cath NORTON PERFORMANCE PLASTICS CORP. k820229 02/12/1982
abuscreen radioimmunoassay for cannabi HOFFMANN-LA ROCHE, INC. k820391 03/08/1982

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