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FDA 510(k) Applications Submitted by SUNSCOPE INTL., INC.
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.
K002786
09/07/2000
BIOSENSORS CENTRAL VENOUS CATHETER KITS
SUNSCOPE INTL., INC.
K983372
09/24/1998
BIOPORT CLOSED BLOOD SAMPLING SYSTEM, MODEL BT XXXXXX- BP
SUNSCOPE INTL., INC.
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