Scion International, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K040087RABBITApril 1, 2004
K973698SCION BALLOON ELEVATORMarch 31, 1998
K973652DUOCLIPPER TITANIUM CLIPSMarch 27, 1998
K963006SCION SAPHENOUS VEIN HARVESTING SYSTEMSeptember 20, 1996