Norland Corp.
Norland Corp. holds FDA 510(k) medical device clearances, first cleared 1979, most recent 1998.
Top product codes for Norland Corp.
Recent clearances by Norland Corp.
- K980289 — FRACTURE RISK ASSESSMENT FOR THE NORLAND SXA 3000 BONE DENSITOMETER
- K980569 — FRACTURE RISK ASSESSMENT CAPABILITY FOR NORLAND X-RAY BONE DENSITOMETERS
- K980125 — REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETER
- K973459 — NORLAND BODY COMPOSITION OPTION FOR NORLAND DEXA BONE DENSITOMETERS
- K973104 — NORLAND MODEL PDEXA BONE DENSITOMETER
- K972882 — APOLLO
- K931996 — MODEL PDEXA BONE DENSITOMETER
- K926019 — FORARM OPT/NORLAND XR SERIES X-RAY BONE DENSITOMET
- K922286 — MODEL XCT-900 PQCT X-RAY BONE DENSITOMETER
- K913078 — LATERAL SPINE OPT. XR-SERIES X-RAY BONE DENSITOMET
- K901804 — NORLAND XR26 WHOLE BODY OPTION
- K902959 — NORLAND XR26 LATERAL SPINE OPTION
- K881865 — NORLAND MODEL XR-26 X-RAY BONE DENSITOMETER
- K841463 — BONE DENSITOMETER
- K792444 — NORLAND MODEL 278 BONE DENSITOMETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.