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Arcadia Medical Corporation

FDA Regulatory Profile

Arcadia Medical Corporation appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 8, 2006.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K060094ARCADIA MEDICAL SILICONE WIRE REINFORCED ENDOTRACHEAL TUBESMay 8, 2006
K031553SILICONE FOAM CUFF TRACHEOSTOMY TUBES, SILICONE CUFFLESS NEONATAL AND PEDIATRIC TRACHEOSTOMY TUBESNovember 18, 2003

FDA data resources