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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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corning 2500 co-oximeter Corning Medical & Scientific k830590 04/05/1983
single use nebulizer, adjust. air- Airlife, Inc. k830895 04/28/1983
e-z fit Triad Medical Division k831287 10/14/1983
multichem enzymatic cholesterol sys Simmler, Inc. k831700 07/19/1983
neuroflax, epk Franks Electronics k831990 11/28/1983
onpg discs Oxoid U.S.A., Inc. k832307 08/26/1983
windsor medical model 52 Windsor Medical, Inc. k832641 10/04/1983
gas chromatograph 5890a Hewlett-Packard Co. k832962 10/28/1983
alpha y-recipient set Alpha Therapeutic Corp. k833294 12/27/1983
betaject bd u100 Orange Medical Instruments, Inc. k833705 05/09/1984

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