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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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mtg - minitub heated stage systems Zander Medical Supplies, Inc. k002971 12/15/2000
merogel control gel ent surgical dressing Medtronic Xomed k002972 12/15/2000
acti-flex fluid delivery system or acti-flex f d s R-Group Intl. k001233 12/13/2000
subdural evacuating port system, model 11-9901 Medical Designs, LLC k002970 12/12/2000
trilogy acetabular system large head liner, model 6353 Zimmer, Inc. k002960 12/11/2000
magellan ventilator Oceanic Medical Products, Inc. k002951 12/08/2000
xltek evoked potential headbox, model ep-8 Xltek k002969 12/08/2000
tcm400 Radiometer Medical A/S k001866 12/07/2000
polaris x catheters, model 7000d,7001d,7003d,7004d,7005d,7006d Ep Technologies, Inc. k003452 12/07/2000
modification to chad therapeutics oxymatic model 401 Chad Therapeutics, Inc. k003455 12/06/2000

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