Summit Medical Products, Inc.
Summit Medical Products, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 29, 2017.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 3
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K162165 | ambIT PCA*PIB, ambIT PIB, ambIT PIB*PCA, ambIT PIEB, and ambIT Programmable Intermittent Pump | August 29, 2017 |
| K113043 | DIRECT ANTIBIOTIC INFUSION KIT | December 20, 2011 |
| K110814 | AMBIT TUNNELER | April 8, 2011 |
| K102460 | AMBIT INTRODUCER, AMBIT NEEDLE, AMBIT SHEATH | January 13, 2011 |