Resonex, Inc.
FDA 510(k) & PMA Approved Devices — 21 products
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Total Devices21
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K935369 | FAST SPIN ECHO (FSE) | LNH | 1994-03-21 | View |
| 510(k) | K935570 | NOISE FILTER FOR PARADIGM MAGNETIC RESONANCE IMAGING SYSTEM | LNH | 1994-03-16 | View |
| 510(k) | K931392 | ECG GATING UNIT | LNH | 1993-11-02 | View |
| 510(k) | K923870 | 3DTOF MRA | LNH | 1993-01-12 | View |
| 510(k) | K924154 | KINEMATIC MRI MOVIEMAKER | LNH | 1992-11-23 | View |
| 510(k) | K923823 | 3D IMAGING | LNH | 1992-10-30 | View |
| 510(k) | K922677 | MAGNETIZATION TRANSFER CONTRAST | LNH | 1992-09-04 | View |
| 510(k) | K920254 | COILS FOR RX4000 & RX5000 MRI SYSTEMS | LNH | 1992-06-22 | View |
| 510(k) | K921046 | BO POWER SUPPLY | LNH | 1992-05-28 | View |
| 510(k) | K920835 | PRESATURATION | LNH | 1992-05-22 | View |
| 510(k) | K915754 | 16 BIT A/D | LNH | 1992-03-16 | View |
| 510(k) | K914114 | 2DTOF MAGNETIC RESONANCE ANGIOGRAPH (MRA) | LNH | 1991-12-04 | View |
| 510(k) | K913325 | 40-140 SPIN ECHO FLOW COMPENSATED PULSE SEQUENCE | LNH | 1991-11-01 | View |
| 510(k) | K911800 | COIL FIELD EXTENDER | LNH | 1991-07-03 | View |
| 510(k) | K911892 | RX-5000 MRI SYSTEM | LNH | 1991-06-20 | View |
| 510(k) | K910269 | 10 ADJUSTABLE BELT COIL | LNH | 1991-04-08 | View |
| 510(k) | K902630 | BILATERAL TMJ COIL | LNH | 1990-07-19 | View |
| 510(k) | K901602 | VERSION 4.3 APPLICATION SOFTWARE FOR USE W/RX-4000 | LNH | 1990-05-07 | View |
| 510(k) | K894974 | MOBILE RX-4000 MAGNETIC RESONANCE IMAGING SYSTEM | LNH | 1989-09-12 | View |
| 510(k) | K892959 | VERSION 4.2 APPLICATION SOFTWARE | LNH | 1989-06-01 | View |
No matching devices.
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