Summit Medical Products, Inc. is one of 18372 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Summit Medical Products, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ambIT PCA*PIB, ambIT PIB, ambIT PIB*PCA, ambIT PIEB, and ambIT Programmable Intermittent Pump, DIRECT ANTIBIOTIC INFUSION KIT, AMBIT TUNNELER
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.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Summit Medical Products, Inc.
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