The following data is part of a premarket notification filed by Maddak, Inc. with the FDA for Arm Sling, Pouch Type.
| Device ID | K812477 |
| 510k Number | K812477 |
| Device Name: | ARM SLING, POUCH TYPE |
| Classification | Sling, Arm |
| Applicant | MADDAK, 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 | 1981-08-31 |
| Decision Date | 1981-09-14 |