Summit Medical Products, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Summit Medical Products, Inc. has 4 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 4 cleared submissions from 2011 to 2017. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Summit Medical Products, Inc. Filter by specialty or product code using the sidebar.
4 devices
Cleared
Aug 29, 2017
ambIT PCA*PIB, ambIT PIB, ambIT PIB*PCA, ambIT PIEB, and ambIT Programmable...
General Hospital
391d
Cleared
Dec 20, 2011
DIRECT ANTIBIOTIC INFUSION KIT
General & Plastic Surgery
68d
Cleared
Apr 08, 2011
AMBIT TUNNELER
Anesthesiology
15d
Cleared
Jan 13, 2011
AMBIT INTRODUCER, AMBIT NEEDLE, AMBIT SHEATH
Anesthesiology
139d