Summit Medical Products, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K162165ambIT PCA*PIB, ambIT PIB, ambIT PIB*PCA, ambIT PIEB, and ambIT Programmable Intermittent PumpAugust 29, 2017
K113043DIRECT ANTIBIOTIC INFUSION KITDecember 20, 2011
K110814AMBIT TUNNELERApril 8, 2011
K102460AMBIT INTRODUCER, AMBIT NEEDLE, AMBIT SHEATHJanuary 13, 2011