Resonex, Inc.
Resonex, Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1994.
Top product codes for Resonex, Inc.
Recent clearances by Resonex, Inc.
- K935369 — FAST SPIN ECHO (FSE)
- K935570 — NOISE FILTER FOR PARADIGM MAGNETIC RESONANCE IMAGING SYSTEM
- K931392 — ECG GATING UNIT
- K923870 — 3DTOF MRA
- K924154 — KINEMATIC MRI MOVIEMAKER
- K923823 — 3D IMAGING
- K922677 — MAGNETIZATION TRANSFER CONTRAST
- K920254 — COILS FOR RX4000 & RX5000 MRI SYSTEMS
- K921046 — BO POWER SUPPLY
- K920835 — PRESATURATION
- K915754 — 16 BIT A/D
- K914114 — 2DTOF MAGNETIC RESONANCE ANGIOGRAPH (MRA)
- K913325 — 40-140 SPIN ECHO FLOW COMPENSATED PULSE SEQUENCE
- K911800 — COIL FIELD EXTENDER
- K911892 — RX-5000 MRI SYSTEM
- K910269 — 10 ADJUSTABLE BELT COIL
- K902630 — BILATERAL TMJ COIL
- K901602 — VERSION 4.3 APPLICATION SOFTWARE FOR USE W/RX-4000
- K894974 — MOBILE RX-4000 MAGNETIC RESONANCE IMAGING SYSTEM
- K892959 — VERSION 4.2 APPLICATION SOFTWARE
- K883737 — VFQ HEAD COIL
Data sourced from openFDA. This site is unofficial and independent of the FDA.