Medical Device Manufacturer · US , Mchenry , IL

Norland Corp. - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 1979

Total

Cleared

Denied

Norland Corp. has 15 FDA 510(k) cleared radiology devices. Based in Mchenry, US.

Historical record: 15 cleared submissions from 1979 to 1998.

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 - Norland Corp.

15 devices

1-12 of 15

Cleared Jun 12, 1998

FRACTURE RISK ASSESSMENT FOR THE NORLAND SXA 3000 BONE DENSITOMETER

K980289 · KGI

Radiology · 137d

Cleared Jun 12, 1998

FRACTURE RISK ASSESSMENT CAPABILITY FOR NORLAND X-RAY BONE DENSITOMETERS

K980569 · KGI

Radiology · 119d

Cleared May 20, 1998

REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETER

K980125 · KGI

Radiology · 126d

Cleared Feb 13, 1998

NORLAND BODY COMPOSITION OPTION FOR NORLAND DEXA BONE DENSITOMETERS

K973459 · KGI

Radiology · 154d

Cleared Jan 29, 1998

NORLAND MODEL PDEXA BONE DENSITOMETER

MODEL PDEXA BONE DENSITOMETER

K931996 · KGI

Radiology · 649d

Cleared Sep 23, 1994

FORARM OPT/NORLAND XR SERIES X-RAY BONE DENSITOMET

K926019 · KGI

Radiology · 662d

Cleared Nov 27, 1992

MODEL XCT-900 PQCT X-RAY BONE DENSITOMETER

K922286 · KGI

Radiology · 196d

Cleared Sep 24, 1991

LATERAL SPINE OPT. XR-SERIES X-RAY BONE DENSITOMET

K913078 · KGI

Radiology · 75d

Cleared Apr 29, 1991

NORLAND XR26 WHOLE BODY OPTION

K901804 · KGI

Radiology · 374d

Cleared Nov 23, 1990

NORLAND XR26 LATERAL SPINE OPTION

K902959 · KGI

Radiology · 141d

Norland Corp. - FDA 510(k) Cleared Devices

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