Product code LXC— Unknown
MY01 Continuous Compartmental Pressure Monitor
- Classification name
- Monitor, Pressure, Intracompartmental
- Device class
- Unclassified
- Advisory panel
- Unknown
- Total cleared
- 15
- First cleared
- Most recent
Market context for product code LXC
FDA has cleared devices under product code LXC between 1985 and 2026, filed by 8 applicant companies. No FDA device recalls reference this product code.
Clearances per year
- 2026
- 2025
- 2023
- 2022
- 2021
- 2020
- 2014
- 2009
- 2006
- 2004
- 2003
- 1988
- 1985
Top applicants under product code LXC
Recent clearances under product code LXC
- K251900 — MY01 Continuous Compartmental Pressure Monitor
- K242997 — MY01 Continuous Compartmental Pressure Monitor
- K223509 — Compremium Compartment Compressibility Monitoring System (CPM#1)
- K220952 — MY01 Continuous Compartmental Pressure Monitor
- K210525 — MY01 Continuous Compartmental Pressure Monitor
- K202635 — MY01 Continuous Compartmental Pressure Monitor
- K193321 — MY01 Continuous Compartmental Pressure Monitor
- K131966 — TWIN STAR EXTREMITY COMPARTMENT SYNDROME MONITOR AND FLUID COLLECTION CATHETER SYSTEM
- K090961 — TWIN STAR COMPARTMENT PRESSURE MONITOR AND FLUID COLLECTION CATHETER SYSTEM (CMS-II)
- K060963 — TWIN STAR COMPARTMENT PRESSURE MONITORING AND FLUID COLLECTION MONITOR (CMS MONITOR)
- K041771 — TWIN STAR COMPARTMENT SYNDROME PRESSURE MONITORING AND FLUID COLLECTION CATHETER SYSTEM
- K031555 — SYNTHES (USA) COMPARTMENTAL PRESSURE MONITORING SYSTEM
- K881858 — ACE ICPM SIDE PORTED NEEDLE
- K873684 — ACE INTRA COMPARTMENTAL PRESSURE MONITOR
- K844214 — COMPARTMENT SYNDROME PRESSURE MONITOR SYS
Data sourced from openFDA. This site is unofficial and independent of the FDA.