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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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ria sys. for human growth hormone CALBIOCHEM-BEHRING CORP. k780347 04/12/1978
pressure modules models 1855 & 1856 LIFE-TECH INSTRUMENTS, INC. k780541 05/19/1978
central catheter kit ARGON MEDICAL CORP. k780673 05/16/1978
draping material, colbalt 60 sterile KIMBERLY-CLARK CORP. k780846 06/19/1978
otoscope, diag. models 20100 & 20200 WELCH ALLYN, INC. k781029 06/28/1978
infusion, venothin 23 VENOSPITAL, INC. k781186 08/10/1978
cast shoe CUTLER BIOMEDICAL k781363 08/14/1978
trauma drainage set 72t-32ttc SORENSEN RESEARCH k781551 10/26/1978
phipiological synchronizer part#205 BRATTLE INSTRUMENT CORP. k781681 10/17/1978
adapter, catheter sheath ARROW INTL., INC. k781846 12/12/1978

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