The following data is part of a premarket notification filed by Warm & Form, Orthopedic Materials with the FDA for Universal Sling, Sling & Swathe.
| Device ID | K823162 |
| 510k Number | K823162 |
| Device Name: | UNIVERSAL SLING, SLING & SWATHE |
| Classification | Sling, Arm |
| Applicant | WARM & FORM, ORTHOPEDIC MATERIALS 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 | 1982-10-25 |
| Decision Date | 1982-11-10 |