The following data is part of a premarket notification filed by Fred Sammons, Inc. with the FDA for Arm Slings.
| Device ID | K831549 |
| 510k Number | K831549 |
| Device Name: | ARM SLINGS |
| Classification | Sling, Arm |
| Applicant | FRED SAMMONS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | ILI |
| CFR Regulation Number | 890.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-05-12 |
| Decision Date | 1983-06-30 |