Surefire Medical, Inc.
Surefire Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2018.
Top product codes for Surefire Medical, Inc.
Recent clearances by Surefire Medical, Inc.
- K180677 — Surefire Spark Infusion System
- K171355 — Surefire Precision Infusion System
- K162359 — Surefire Guiding Catheter
- K160662 — Surefire Infusion System
- K143588 — Surefire Infusion System 021
- K140034 — SUREFIRE GUIDING CATHETER
- K122506 — SUREFIRE HIGH FLOW ANGIOGRAPHIC CATHETER, ACCESS
- K121677 — SUREFIRE HI-FLOW MICROCATHETER
- K113737 — SUREFIRE GUIDE SHEATH
- K110459 — SUREFIRE INFUSION CATHETER SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.