Pathfinder Therapeutics, Inc.

FDA Regulatory Profile

Pathfinder Therapeutics, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 9, 2011.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K101979EXPLORER LIVER (PASSIVE TRACKING)February 9, 2011
K093494LINASYS IMAGE-GUIDED LIVER SURGERY SYSTEMMarch 30, 2010
K082228PLANISIGHT LINASYSSeptember 22, 2008
K071063LINASYSDecember 20, 2007