Medical Device Manufacturer · US , Sunnyvale , CA

Resonex, Inc. - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 1988

Total

Cleared

Denied

Resonex, Inc. has 21 FDA 510(k) cleared radiology devices. Based in Sunnyvale, US.

Historical record: 21 cleared submissions from 1988 to 1994.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Resonex, Inc.

21 devices

1-12 of 21

NOISE FILTER FOR PARADIGM MAGNETIC RESONANCE IMAGING SYSTEM

KINEMATIC MRI MOVIEMAKER

MAGNETIZATION TRANSFER CONTRAST

K922677 · LNH

Radiology · 92d

Cleared Jun 22, 1992

COILS FOR RX4000 & RX5000 MRI SYSTEMS

2DTOF MAGNETIC RESONANCE ANGIOGRAPH (MRA)

K914114 · LNH

Radiology · 82d

Resonex, Inc. - FDA 510(k) Cleared Devices

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