Medical Device Manufacturer · US , Mchenry , IL

Cgr Medical Corp. - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 1978

Total

Cleared

Denied

Cgr Medical Corp. has 20 FDA 510(k) cleared radiology devices. Based in Mchenry, US.

Historical record: 20 cleared submissions from 1978 to 1984.

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 - Cgr Medical Corp.

20 devices

1-12 of 20

PHASIX-HIGH FREQUENCY GENERATOR

SATURNE I LINEAR ACCELERATOR

K837412

Radiology · 68d

Cleared Jun 28, 1983

ALCYON ROTATIONAL COBALT THERAPY

K837465

Radiology · 56d

Cleared Apr 29, 1983

VERASUN RADIATION THERAPY SIMULATION SYSTEM

K837336

Radiology · 30d

Cleared Nov 04, 1982

HYPERLUX 30 IMAGE SYSTEM

K827489 · JAA

Radiology

Cgr Medical Corp. - FDA 510(k) Cleared Devices

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