The following data is part of a premarket notification filed by E.m. Adams with the FDA for Leaded X-ray Apron.
| Device ID | K832601 |
| 510k Number | K832601 |
| Device Name: | LEADED X-RAY APRON |
| Classification | Apron, Leaded |
| Applicant | E.M. ADAMS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EAJ |
| CFR Regulation Number | 892.6500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-08-02 |
| Decision Date | 1983-09-29 |