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U.S. Department of Health and Human Services

510(K) Premarket Notification
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261 to 270 of 500 Results *
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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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modification to m2376a devicelink system PHILIPS MEDICAL SYSTEMS, INC. k013470 11/14/2001
delta 2000 series extracorporeal lithotripter E.S.W.L. PRODUCTS, INC. k013471 04/29/2002
total o2 CHAD THERAPEUTICS, INC. k013472 11/28/2001
xtd thrombectomy catheter, xx cm, model# ct000500x; xtd control console, model # ct0006001; xtd collection bottle, model XTRAK MEDICAL INC. k013473 03/06/2002
trident porous titanium acetabular component with peri-apatite coating HOWMEDICA OSTEONICS CORP. k013475 12/20/2001
toco lite, model td-01 VENTREX, INC. k013477 01/17/2002
dynapulse 5200a pathway blood pressure monitoring system PULSE METRIC, INC. k013478 01/10/2002
complete brand multi-purpose solution ALLERGAN, INC. k013479 02/11/2002
cobe smarxt optimin surface modified hollow fiber membrane oxygenator COBE CARDIOVASCULAR, INC. k013480 11/16/2001
dual energy and tissue equalization software option GE MEDICAL SYSTEMS k013481 11/02/2001

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