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P.T. Greenleaf

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K020419V SETAugust 29, 2003
K020418GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICESApril 29, 2003