The following data is part of a premarket notification filed by American Thermal Instruments, Inc. with the FDA for Breast & Body Health System 2000.
| Device ID | K832731 |
| 510k Number | K832731 |
| Device Name: | BREAST & BODY HEALTH SYSTEM 2000 |
| Classification | System, Thermographic, Liquid Crystal, Powered (adjunctive Use) |
| Applicant | AMERICAN THERMAL INSTRUMENTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KXZ |
| CFR Regulation Number | 884.2982 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-08-04 |
| Decision Date | 1984-01-30 |