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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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microsurg cautery MEDICAL PRODUCTS DEVELOPMENT, INC. k810017 01/05/1981
bone-dri surgical sponge HOWMEDICA CORP. k803125 01/15/1981
dca digox-syn ria test DIAGNOSTIC CORP. OF AMERICA k810477 03/11/1981
respiration function blocks HONEYWELL, INC. k810174 03/17/1981
api turbicity standard ANALYTICAL PRODUCTS, INC. k810762 04/03/1981
depuy segmentalspinal system DEPUY, INC. k810329 04/08/1981
implantable programmable cardiac pulse TELECTRONICS, INC. k810603 04/14/1981
model 533 phototherapy unit NARCO AIR-SHIELDS k810953 04/23/1981
dade rpr card test AMERICAN DADE k811152 05/15/1981
model 5866-24 lead adaptor kit MEDTRONIC VASCULAR k811349 06/30/1981

*   The maximum 500 records meeting your search criteria returned. Please narrow your search.
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