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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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endoscope and accessories OLYMPUS CORP. k790071 04/02/1979
electrocardiograph, at-300 3 channel HEALTH TECHNOLOGY LABORATORIES, INC. k790233 02/08/1979
ultrasonic diagnostic system HOFFREL INSTRUMENTS, INC. k790396 03/21/1979
aortic root cannula DLP, INC. k790565 06/11/1979
reagent system #350hdl, sigma procedure SIGMA CHEMICAL CO. k790760 05/23/1979
bordispo brand hypodermic needle BORDA PRODUCTS, INC. k790953 06/27/1979
acta-scanner 0220fs PFIZER, INC. k791153 08/03/1979
adr-10600(adr 400),10601 (adr 300) PHYSIO-CONTROL CORP. k791342 11/16/1979
model 344 TELEX COMMUNICATIONS, INC. k791506 09/19/1979
immuchem covalent coat solid phase assay IMMUCHEM CORP. k791663 10/01/1979

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