The following data is part of a premarket notification filed by Alimed, Inc. with the FDA for Total Finger Flexion Splint.
| Device ID | K822651 |
| 510k Number | K822651 |
| Device Name: | TOTAL FINGER FLEXION SPLINT |
| Classification | Splint, Hand, And Components |
| Applicant | ALIMED, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | ILH |
| CFR Regulation Number | 890.3475 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-09-02 |
| Decision Date | 1982-09-17 |