Resonex, Inc.
Sunnyvale, CA, US
Resonex, Inc. appears in FDA device records in Sunnyvale, CA. FDA records list 21 510(k) clearances between and , 2 PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 21
- PMA records
- 2
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 21 510(k) clearances for Resonex, Inc. between 1988 and 1994. The busiest year on record is 1992, with 7. The most recent is 1994, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1988 | 1 |
| 1989 | 2 |
| 1990 | 2 |
| 1991 | 5 |
| 1992 | 7 |
| 1993 | 2 |
| 1994 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K935369 | FAST SPIN ECHO (FSE) | LNH | Substantially Equivalent | |
| K935570 | NOISE FILTER FOR PARADIGM MAGNETIC RESONANCE IMAGING SYSTEM | LNH | Substantially Equivalent | |
| K931392 | ECG GATING UNIT | LNH | Substantially Equivalent | |
| K923870 | 3DTOF MRA | LNH | Substantially Equivalent | |
| K924154 | KINEMATIC MRI MOVIEMAKER | LNH | Substantially Equivalent | |
| K923823 | 3D IMAGING | LNH | Substantially Equivalent | |
| K922677 | MAGNETIZATION TRANSFER CONTRAST | LNH | Substantially Equivalent | |
| K920254 | COILS FOR RX4000 & RX5000 MRI SYSTEMS | LNH | Substantially Equivalent | |
| K921046 | BO POWER SUPPLY | LNH | Substantially Equivalent | |
| K920835 | PRESATURATION | LNH | Substantially Equivalent | |
| K915754 | 16 BIT A/D | LNH | Substantially Equivalent | |
| K914114 | 2DTOF MAGNETIC RESONANCE ANGIOGRAPH (MRA) | LNH | Substantially Equivalent | |
| K913325 | 40-140 SPIN ECHO FLOW COMPENSATED PULSE SEQUENCE | LNH | Substantially Equivalent | |
| K911800 | COIL FIELD EXTENDER | LNH | Substantially Equivalent | |
| K911892 | RX-5000 MRI SYSTEM | LNH | Substantially Equivalent | |
| K910269 | 10 ADJUSTABLE BELT COIL | LNH | Substantially Equivalent | |
| K902630 | BILATERAL TMJ COIL | LNH | Substantially Equivalent | |
| K901602 | VERSION 4.3 APPLICATION SOFTWARE FOR USE W/RX-4000 | LNH | Substantially Equivalent | |
| K894974 | MOBILE RX-4000 MAGNETIC RESONANCE IMAGING SYSTEM | LNH | Substantially Equivalent | |
| K892959 | VERSION 4.2 APPLICATION SOFTWARE | LNH | Substantially Equivalent | |
| K883737 | VFQ HEAD COIL | LNH | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain