Medical Device Manufacturer · US , Mchenry , IL

General X-Ray, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1978

Total

Cleared

Denied

General X-Ray, Inc. has 14 FDA 510(k) cleared radiology devices. Based in Mchenry, US.

Historical record: 14 cleared submissions from 1978 to 1980.

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

General X-Ray, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - General X-Ray, Inc.

14 devices

1-14 of 14

Cleared May 28, 1980

ATLAS-S X-RAY SYSTEM W/KETROMAT GEN.

K800998

Radiology · 33d

Cleared Mar 28, 1979

X-RAY UNITS, GX-101, UCIS-510 AND GX-111

K790451 · IZL

Radiology · 23d

Cleared Mar 26, 1979

510 CARBINETTE X-RAY UNIT

K790392 · IZL

Radiology · 28d

Cleared Mar 26, 1979

PORTABLE X-RAY UNIT, MATRIX S GX-101

X-RAY STAND, PORTABLE

X-RAY UNIT, PORTABLE GX-101 AEC

General X-Ray, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - General X-Ray, Inc.

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