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Vascucare, Inc.

FDA Regulatory Profile

Summary

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

Known Names

vascu-care, vascucare

Recent 510(k) Clearances

K-NumberDeviceDate
K890047VASCUCARE PERCUTANEOUS ANGIOSCOPY DELIVERY SYSTEMJune 20, 1989
K883158RESPIRATORY AIRWAY TUBE MONITOR (RATM)March 6, 1989
K881780VASCUCARE ANGIOPUMPSeptember 28, 1988