Sunscope Intl., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K002786BIOSENSORS CENTRAL VENOUS CATHETER KITSNovember 17, 2000
K983372BIOPORT CLOSED BLOOD SAMPLING SYSTEM, MODEL BT XXXXXX- BPFebruary 5, 1999
K973477BIOSENSORS EMBOLECTOMY CATHETERSeptember 4, 1998
K981747BIOTRANS PRESSURE MONITORING KIT MODEL NUMBER BT XXXXXXAugust 20, 1998
K981745BIOTRANS REUSABLE SENSOR BASE MODEL NUMBER BT XXXXXXJuly 17, 1998
K911710HEPARIN COATED THERMODILUTION CATH & ACCESSORIESOctober 23, 1991
K912172SAFEWEDGE(TM) RELIEF VALVE DEVICESeptember 27, 1991