Norland Corp.
FDA 510(k) & PMA Approved Devices — 15 products
Advertisement
Total Devices15
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K980569 | FRACTURE RISK ASSESSMENT CAPABILITY FOR NORLAND X-RAY BONE DENSITOMETERS | KGI | 1998-06-12 | View |
| 510(k) | K980289 | FRACTURE RISK ASSESSMENT FOR THE NORLAND SXA 3000 BONE DENSITOMETER | KGI | 1998-06-12 | View |
| 510(k) | K980125 | REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETER | KGI | 1998-05-20 | View |
| 510(k) | K973459 | NORLAND BODY COMPOSITION OPTION FOR NORLAND DEXA BONE DENSITOMETERS | KGI | 1998-02-13 | View |
| 510(k) | K973104 | NORLAND MODEL PDEXA BONE DENSITOMETER | KGI | 1998-01-29 | View |
| 510(k) | K972882 | APOLLO | KGI | 1997-10-31 | View |
| 510(k) | K931996 | MODEL PDEXA BONE DENSITOMETER | KGI | 1995-02-01 | View |
| 510(k) | K926019 | FORARM OPT/NORLAND XR SERIES X-RAY BONE DENSITOMET | KGI | 1994-09-23 | View |
| 510(k) | K922286 | MODEL XCT-900 PQCT X-RAY BONE DENSITOMETER | KGI | 1992-11-27 | View |
| 510(k) | K913078 | LATERAL SPINE OPT. XR-SERIES X-RAY BONE DENSITOMET | KGI | 1991-09-24 | View |
| 510(k) | K901804 | NORLAND XR26 WHOLE BODY OPTION | KGI | 1991-04-29 | View |
| 510(k) | K902959 | NORLAND XR26 LATERAL SPINE OPTION | KGI | 1990-11-23 | View |
| 510(k) | K881865 | NORLAND MODEL XR-26 X-RAY BONE DENSITOMETER | KGI | 1989-03-14 | View |
| 510(k) | K841463 | BONE DENSITOMETER | KGI | 1984-07-17 | View |
| 510(k) | K792444 | NORLAND MODEL 278 BONE DENSITOMETER | KGI | 1979-12-27 | View |
No matching devices.
Advertisement