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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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respirgard MARQUEST MEDICAL PRODUCTS, INC. k802763 11/26/1980
oricult dtm ORION DIAGNOSTICA, INC. k802947 12/22/1980
ames tda amikacin control serum MILES LABORATORIES, INC. k803107 12/22/1980
osteo oscilair RICHARD'S MEDICAL EQUIP., INC. k803284 01/09/1981
iso-bac instrument wrap AMERICAN CONVERTORS DIV., AMERICAN PHARMASEAL k802919 02/02/1981
isorobic skinfold caliper FITNESS MOTIVATION INSTITUTE OF AMERICA k810116 02/04/1981
zonograph 6 SIEMENS CORP. k810307 03/11/1981
support SCI-PHARM, INC. k810479 03/17/1981
cytobucket model 1024 CYTOCHEM, INC. k810848 04/23/1981
sterility test broth ACUMEDIA MANUFACTURERS, INC. k811046 05/05/1981

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