K890999 is an FDA 510(k) clearance for the MODIFIED QDR-1000 X-RAY BONE DENSITOMETER. This device is classified as a Densitometer, Bone (Class II - Special Controls, product code KGI).
Submitted by Hologic, Inc. (Waltham, US). The FDA issued a Cleared decision on December 21, 1989, 297 days after receiving the submission on February 27, 1989.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1170.
| 510(k) Number | K890999 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 27, 1989 |
| Decision Date | December 21, 1989 |
| Days to Decision | 297 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | — |
| Product Code | KGI — Densitometer, Bone |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1170 |