Computerized Medical Systems, Inc.
Computerized Medical Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 1985, most recent 2011.
Top product codes for Computerized Medical Systems, Inc.
Recent clearances by Computerized Medical Systems, Inc.
- K110730 — MONACO RTP SYSTEM
- K102216 — XIO RTP SYSTEM
- K092132 — XIO RTP SYSTEM
- K091179 — MONACO RTP SYSTEM, VMAT OPTION
- K080799 — ATLAS-BASED AUTOSEGMENTATION
- K071938 — MONACO RTP SYSTEM
- K032762 — XIO RADIATION TREATMENT PLANNING SYSTEM
- K032100 — I-BEAM
- K020027 — FOCUS RADIATION TREATMENT PLANNING SYSTEM
- K013112 — FOCAL SIM
- K002147 — FOCUS
- K000137 — ENHANCED COMPENSATING FILTER
- K981535 — FOCUS PILOT CONTOURING WORKSTATION
- K973936 — FOCUS RTP SYSTEM
- K915691 — FOCUS RTP
- K921108 — CMS RECORD AND VERIFY
- K913674 — RECORD AND VERIFY MEVATRON ADAPTER
- K913017 — MODULEX RTP SYSTEM
- K882484 — CMS RECORD AND VERIFY SYSTEM
- K863535 — LIFE-TRACE 18 SINGLE-TRACE CARDIAC MONITOR/RECORD.
- K863534 — LIFE-WATCH MONITOR LT-8
- K854880 — RADIATION BEAM DATA ACQUISTIOIN SYSTEMS
- K853964 — COMPUTERIZED RADIATION TREATMENT PLANNING SYS
Data sourced from openFDA. This site is unofficial and independent of the FDA.