K883360 is an FDA 510(k) clearance for the HOLOGIC MODEL WHF-1 ANTHROPOMORPHIC FEMUR PHANTOM. 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 September 27, 1988, 49 days after receiving the submission on August 9, 1988.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1170.
| 510(k) Number | K883360 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 09, 1988 |
| Decision Date | September 27, 1988 |
| Days to Decision | 49 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 |