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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