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Endovascular, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K931421DISPOSABLE STEERABLE ANGIOSCOPEJune 16, 1993
K924075DISPOSABLE OPTICAL VALVULOTOMEFebruary 8, 1993
K923996DISPOSABLE VASCULAR ANGIOSCOPEJanuary 13, 1993