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Catheter Research C/O Burditt, Bowles & Radzius

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K924227CRI CYNOSAR CATHETERJune 29, 1993
K924125CRI ELECTRONIC CONTROL SYSTEMMay 26, 1993
K914523CRI VESSEL OCCLUSIN SYSTEM/CRI OCCLUSION COILJanuary 10, 1992
K904785CRI CYNOSAR CATHETERMarch 6, 1991
K904787CRI STEERABLE CATHETER CONTROL SYSTEMDecember 17, 1990
K900320CRI CYNOSAR CATHETERSeptember 14, 1990
K884337MICRO-GUIDE SYSTEMJanuary 5, 1989
K870700MICRO-GUIDEDecember 3, 1987