Medical Device Manufacturer · US , Hartland , WI

Midwest Rf, LLC - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2000

Total

Cleared

Denied

Midwest Rf, LLC has 9 FDA 510(k) cleared medical devices. Based in Hartland, US.

Historical record: 9 cleared submissions from 2000 to 2011. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Midwest Rf, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Midwest Rf, LLC

9 devices

1-9 of 9

MEP-90 HAIR GROWTH STIMULATION SYSTEM

K091496 · OAP

General & Plastic Surgery · 279d

Cleared Mar 16, 2009

SV DBS BRAIN ARRAY, MODEL 1500SV-SMS64

K090267 · MOS

Radiology · 41d

Cleared Aug 02, 2005

SPECIAL PROCEDURES II HEAD COIL, MODEL 1400GE-64

K051618 · MOS

Radiology · 46d

Cleared Mar 25, 2003

MODEL 1300GE-64: PEDIATRIC POSITIONER

K030317 · MOS

Radiology · 54d

Cleared Dec 28, 2000

BRAIN COIL, MODEL 9800GE-64

K003097 · MOS

Radiology · 86d

Cleared Dec 28, 2000

SPECIAL PROCEDURES HEAD COIL

K003386 · MOS

Radiology · 58d

Cleared Nov 22, 2000

MODEL 6900GE-64: C-SPINE ARRAY

K002860 · MOS

Radiology · 70d

Cleared Nov 21, 2000

MODEL 6600GE-64: TRAMA NECK ARRAY

K002864 · MOS

Radiology · 69d

Midwest Rf, LLC - FDA 510(k) Cleared Devices

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