Company ยท US
Norland Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1979 to 1998. Name variants (Inc, Corp, punctuation) are merged.
15510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| KGI | Densitometer, Bone | 15 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jun 12, 1998 | K980569 | FRACTURE RISK ASSESSMENT CAPABILITY FOR NORLAND X-RAY BONE DENSITOMETERS Norland Corp. | KGI |
| Jun 12, 1998 | K980289 | FRACTURE RISK ASSESSMENT FOR THE NORLAND SXA 3000 BONE DENSITOMETER Norland Corp. | KGI |
| May 20, 1998 | K980125 | REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETER Norland Corp. | KGI |
| Feb 13, 1998 | K973459 | NORLAND BODY COMPOSITION OPTION FOR NORLAND DEXA BONE DENSITOMETERS Norland Corp. | KGI |
| Jan 29, 1998 | K973104 | NORLAND MODEL PDEXA BONE DENSITOMETER Norland Corp. | KGI |
| Oct 31, 1997 | K972882 | APOLLO Norland Corp. | KGI |
| Feb 1, 1995 | K931996 | MODEL PDEXA BONE DENSITOMETER Norland Corp. | KGI |
| Sep 23, 1994 | K926019 | FORARM OPT/NORLAND XR SERIES X-RAY BONE DENSITOMET Norland Corp. | KGI |
| Nov 27, 1992 | K922286 | MODEL XCT-900 PQCT X-RAY BONE DENSITOMETER Norland Corp. | KGI |
| Sep 24, 1991 | K913078 | LATERAL SPINE OPT. XR-SERIES X-RAY BONE DENSITOMET Norland Corp. | KGI |
| Apr 29, 1991 | K901804 | NORLAND XR26 WHOLE BODY OPTION Norland Corp. | KGI |
| Nov 23, 1990 | K902959 | NORLAND XR26 LATERAL SPINE OPTION Norland Corp. | KGI |
| Mar 14, 1989 | K881865 | NORLAND MODEL XR-26 X-RAY BONE DENSITOMETER Norland Corp. | KGI |
| Jul 17, 1984 | K841463 | BONE DENSITOMETER Norland Corp. | KGI |
| Dec 27, 1979 | K792444 | NORLAND MODEL 278 BONE DENSITOMETER Norland Corp. | KGI |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||