The following data is part of a premarket notification filed by Warm & Form, Orthopedic Materials with the FDA for Universal Wrist Splint & Forearm Splint.
Device ID | K823666 |
510k Number | K823666 |
Device Name: | UNIVERSAL WRIST SPLINT & FOREARM SPLINT |
Classification | Splint, Hand, And Components |
Applicant | WARM & FORM, ORTHOPEDIC MATERIALS 4221 Richmond Rd., N.W. Walker, MI 49534 |
Product Code | ILH |
CFR Regulation Number | 890.3475 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-12-06 |
Decision Date | 1982-12-30 |