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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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Applicant
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510(K)
Number
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Decision
Date
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super-sorber HOME HEALTHCARE PRODUCTS, INC. k780938 12/15/1978
ponceau s ELECTROPHORESIS CORP. OF AMERICA k781123 08/10/1978
peep/cpap valve VICKERS AMERICA MEDICAL CORP. k781332 10/04/1978
the visual speech aid EXETER MEDICAL LABS, INC. k781522 11/08/1978
adapter, c/d suction NOVAMETRIX MEDICAL SYSTEMS, INC. k781713 12/12/1978
ria kit, quantitope ige KALLESTAD LABORATORIES, INC. k781904 02/08/1979
stockinette, disposablesurgical ANAGO, INC. k782091 01/10/1979
sterile suction catheter w/control CHESIRE LABORATORIES k770233 04/05/1977
analyzeo, plasma, blood, colysagraph DAMON CORP. k770606 05/06/1977
splint, cockup ORTHOPEDIC SYSTEMS, INC. k770890 05/26/1977

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