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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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graft, cooley guideline, sterile MEADOX MEDICALS, DIV. BOSTON SCIENTIFIC CORP. k760090 07/20/1976
liberator/stroller BURDITT & CALKINS-SIEMENS-ELEMA k760787 10/22/1976
sheet metal clamp FRED SAMMONS, INC. k761119 12/02/1976
neomycin agar with 5% sheep blood BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC k761359 01/14/1977
electrical shock device EDWARD V. KAUFHOLZ, SR. k760462 03/01/1977
hood, clarion surgeons SHERWOOD MEDICAL INDUSTRIES k770261 03/01/1977
piggyback venoset w/0.22 filter ABBOTT LABORATORIES k770518 04/29/1977
aerosol effusion system #1740 HUDSON OXYGEN THERAPY SALES CO. k770771 06/02/1977
x-ray diag. table dt-kcs TOSHIBA MEDICAL SYSTEMS k771293 08/03/1977
cardiozyme ck-control abnormal DADE, BAXTER TRAVENOL DIAGNOSTICS, INC. k770971 08/04/1977

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