The following data is part of a premarket notification filed by Lunar Radiation Corp. with the FDA for Wisconsin Dual-photon Bone Analyzer.
| Device ID | K802180 |
| 510k Number | K802180 |
| Device Name: | WISCONSIN DUAL-PHOTON BONE ANALYZER |
| Classification | Densitometer, Bone |
| Applicant | LUNAR RADIATION CORP. WI |
| Product Code | KGI |
| CFR Regulation Number | 892.1170 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-09-09 |
| Decision Date | 1980-12-31 |