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FDA 510(k) Applications Submitted by JOHN SHULZE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K981745
05/18/1998
BIOTRANS REUSABLE SENSOR BASE MODEL NUMBER BT XXXXXX
SUNSCOPE INTL., INC.
K981747
05/18/1998
BIOTRANS PRESSURE MONITORING KIT MODEL NUMBER BT XXXXXX
SUNSCOPE INTL., INC.
K973477
09/15/1997
BIOSENSORS EMBOLECTOMY CATHETER
SUNSCOPE INTL., INC.
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